Nordent Manufacturing, Inc.
by Nordent Manufacturing Inc. 166 variants
Ref Nordent Diagnostic CatalogueModel REPCNAB2
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 | Number0840018607552SB 00840018607552 | Date23 Feb 2026 | StatusActive |
| United States | GUDID listing GUDID | Number00840018607552 | Date27 May 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- Withdrawn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
- Periodontal probe, reusable
- Model / Reference
- REPCNAB2, Nordent Diagnostic Catalogue
- Primary DI / UDI-DI
- 00840018607552
- Basic UDI-DI
- 0840018607552SB
- FDA Product Code
- EIX
- EMDN Code
- L159003 Dental and periodontal probes and explorers, reusable
- GMDN Term
- Periodontal probe, 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 (19)
- 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
- 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