Notified Body – CE (NB 3038)

USB Certification is a Notified Body recognized by the European Union under TURKAK accreditation with the number NB 3038. It provides CE conformity assessment services under the Personal Protective Equipment Regulation (EU) 2016/425.

Notified Body
(What is a Notified Body?

A Notified Body is an independent body formally authorized by EU legislation to carry out third-party conformity assessment on specific product groups. These organizations are identified in the European Commission’s NANDO database by a four-digit number, which for USB Certification is 3038.

When you see the number “3038” next to the CE marking, it means that the conformity assessment of the relevant product has been carried out by USB Certification. This structure allows the tests performed by laboratories to be integrated directly into a Notified Body file; the bridge between the test report and the CE certificate becomes clear.

Accreditation

TĂśRKAK is accredited under EN ISO/IEC 17065:2012; conformity assessment processes are carried out within the framework of this standard.

NANDO Registration

It is listed in the European Union NANDO system with the number NB 3038; next to the CE marking, this number indicates USB Certification.

Scope

Authorized to conduct conformity assessment under the Personal Protective Equipment Regulation (EU) 2016/425; acts as NB 3038 in CE processes.

NB 3038 – The Role of the Laboratory in CE Processes

Notified Body – The CE (NB 3038) Product Standard evaluates products in five main categories and sets basic criteria for each category.

Within the scope of NB 3038, USB Certification manages product type examination, certification and surveillance processes in accordance with EN ISO/IEC 17065:2012. Test results are evaluated together with the technical file and risk analysis.

It evaluates the test reports from its own laboratories and laboratories it cooperates with, together with the manufacturer’s technical file and risk analysis. The laboratory output is directly linked to the conformity assessment file.

Your test reports become qualified input that can be used in dossiers leading directly to CE marking. Designing conformity assessment and test plans integrated from the beginning reduces revision duplication on the manufacturer and laboratory side.

When preparing the test plan, it is necessary to align with the module structure (e.g. Type Examination, Unit Verification) and Notified Body procedures (such as USB’s UOP-NB procedure). This alignment directly affects file acceptance and process speed.

Traceability of test results, measurement uncertainty, instrument calibrations and laboratory accreditation are critical review topics in file evaluation by NB.

Run Your Test Plan Integrated with NB 3038

Get a free pre-assessment for Notified Body – CE (NB 3038) product certification from our expert team and let us map out your circular design roadmap.

CE – NB 3038 Scope and Infrastructure of USB Certification

EN ISO/IEC 17065 + NB 3038 + EU 2016/425

USB Certification’s Notified Body structure is defined in NANDO and public sources as follows: TURKAK accredited under EN ISO/IEC 17065:2012. Listed in the European Union NANDO system with the number NB 3038. It has announced with official announcements that it has extended its authorization under the Personal Protective Equipment Regulation ( EU) 2016/425.

In the accreditations page and corporate communication, NB 3038 is counted among the core competence areas of USB Certification together with laboratory, industrial certification, inspection and inspection services.

Conformity Assessment Modules

USB Certification implements the following two main conformity assessment modules in accordance with the EU 2016/425 PPE Regulation under NB 3038.

Module B – EU Type Examination
(Annex V)

The technical file of the product, design verification and all necessary tests are carried out in our laboratory.

Module C2 – Production Control + Random Product Checks (Annex VII)

Inspection and surveillance of the conformity of the production process to the approved type; control by random sampling of products going on the market.

Product Scope

PPE product groups we evaluate under NB 3038:

  • Hand, Arm Protective Equipment
  • Foot, Leg and Slip Protective Equipment
  • Protective Equipment Against Electric Shock
  • Protective Clothing for Welding and Related Processes
  • General Body Protective Equipment (Clothing)
  • Respiratory Protection Equipment
  • Protective Clothing Against Static Electricity
  • Protective Equipment against Falling from Height
  • Equipment Providing Protection Against Heat and Fire (≥100°C)
  • Firefighter Clothes
  • Protective Clothing for Motorcycle Riders
  • High Visibility Clothing
  • Protective Equipment Against Hand Held Chain Saws
  • Equipment to Protect Against the Cold
  • Protective Equipment Against Chemical Agents
  • and more…

How to CE Certification of Personal Protective Equipment?

The CE marking symbolizes conformity with the relevant EU directive or regulation; for some product groups, the Notified Body number is mandatory. For example, in personal protective equipment, the CE marking may be followed by “3038”, indicating that the conformity of the product has been assessed and certified by NB 3038. The NANDO database is the reference source for you to check which Notified Body is authorized for which legislation and product codes.

Notified Body – CE

Documents

Remuneration Procedure
Accredited Organisation Application Form
PPE Regulation Guidelines
Procedure for the Conformity Assessment Programme of a Notified Body
PPE Directive
Accreditation Certificate
Blueguide
Procedure for the Rules Governing the Use of Documents and Logos

Frequently Asked Questions

Publicly available information indicates that the NB 3038 is specifically authorized under the Personal Protective Equipment Regulation (EU) 2016/425; coverage details are listed by product code on the NANDO page. Contact USB Certification for the current scope.

Because for some products, third-party conformity assessment is mandatory for CE marking; the correct design of product tests, together with module selection and documentation, both increases the speed to market of the manufacturer and increases the strategic value of your laboratory service. You can write to USB Certificationfor details.

The first step is to clarify which EU regulation/directive your product falls under and the module requirements. Then the test plan, technical dossier and NB application are set up in an integrated schedule. Contact USB Certificationfor an initial consultation.