Nelaton Catheter
by Integral Medical Products Co., Ltd. 201 variants
Ref ADM12CWTModel AD Hydrophilic Nelaton Catheter, PVC, Tiemann Tip
Active
CE MDR
Valid until
Not listed
FDA recalls
Not applicable
Documents
None linked in EUDAMED
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number697067535IMP2ASNNNSADT1WW 06970675354569 | Date20 May 2026 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device Name
- Nelaton Catheter
- Model / Reference
- AD Hydrophilic Nelaton Catheter, PVC, Tiemann Tip, ADM12CWT
- Primary DI / UDI-DI
- 06970675354569
- Basic UDI-DI
- 697067535IMP2ASNNNSADT1WW
- EMDN Code
- U01010601 Tiemann catheters, self-lubricating
- Device Class
- Class IIa
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- CN-MF-000009217
- Authorised representative
- Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001
Other devices from Integral Medical Products Co., Ltd.
Properties
Other properties (12)
- Implantable: No
- Reusable: 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