Glonel
by Global Medikit Limited 20 variants
Ref 5010245GModel Nelaton catheter
Active
CE MDR
Valid until
No date given
FDA recalls
Not applicable
Documents
None linked in EUDAMED
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number8903545GMLNEC011FL 08903545041267 | Date28 Oct 2026 | StatusActive |
Official records
- EUDAMED public site 8903545GMLNEC011FL
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- Withdrawn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
- Model / reference
- Nelaton catheter, 5010245G
- Primary DI / UDI-DI
- 08903545041267
- Basic UDI-DI
- 8903545GMLNEC011FL
- EMDN code
- U01010502 Nelaton catheters, non self-lubricating
- Device class
- Class IIa
- EU registration type
- Standard device
- EU market of registration
- Portugal
Manufacturer details
- EUDAMED SRN
- IN-MF-000013635
- Authorised representative
- Obelis s.a. BE-AR-000000106
Other devices from Global Medikit Limited
Properties
Other properties (13)
- Sterilise before use: No
- Implantable: No
- Reusable: No
- Contains latex: No
- Reprocessed single-use device: No
- Contains CMR substances (carcinogenic, mutagenic or toxic to reproduction): No
- Incorporates a substance derived from human blood or plasma: No
- Contains human tissues or cells: No
- Contains animal tissues or cells: No
- Contains endocrine-disrupting substances: No
- Administering medicine: No
- Measuring function: No
- Incorporates a medicinal substance: No