Nordent Manufacturing, Inc.
by Nordent Manufacturing Inc. 166 variants
Ref Nordent Catalogue Hygiene SectionModel RECSL84
Active
CE MDR
Valid until
Not listed
FDA recalls
Not checked
Documents
None linked in EUDAMED
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number0840018621885E 00840018642188 | Date30 Oct 2025 | StatusActive |
| United States | GUDID listing GUDID | Number00840018642188 | Date18 Jun 2020 | StatusListed |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Generic Name
- Bone file/rasp, manual, reusable
- Model / Reference
- RECSL84, Nordent Catalogue Hygiene Section
- Primary DI / UDI-DI
- 00840018642188
- Basic UDI-DI
- 0840018621885E
- FDA Product Code
- EMK
- EMDN Code
- L159001 Dental and periodontal curettes, reusable
- GMDN Term
- Bone file/rasp, manual, reusable
- Device Class
- Class I
- Regulation Number
- 872.4565
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
Manufacturer details
- EUDAMED SRN
- US-MF-000048439
- Authorised representative
- Ukens Dental DE-AR-000022084
Other devices from Nordent Manufacturing Inc
Properties
Other properties (20)
- Sterile: No
- Single Use: No
- Implantable: No
- Contains Latex: No
- Reprocessed: No
- CMR Substance: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Endocrine Disruptor: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No
- Prescription Use: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Serial Number: No
- Expiration Date: No