Mediryle
by Global Medikit Limited 10 variants
Ref 5080125Model Ryle’s tube
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 | Number8903545GMLRST009S6 08903545020170 | Date5 Feb 2026 | StatusActive |
Official records
- EUDAMED public site 8903545GMLRST009S6
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- Withdrawn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
- Ryle’s tube
- Model / reference
- Ryle’s tube, 5080125
- Primary DI / UDI-DI
- 08903545020170
- Basic UDI-DI
- 8903545GMLRST009S6
- EMDN code
- G02020101 Nasogastric tubes
- 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 (12)
- 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
- Measuring function: No
- Incorporates a medicinal substance: No