Epi-Guard
Ref 8170
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 |
|---|---|---|---|---|
| United States | GUDID listing GUDID | Number05708265015337 | Date2 Apr 2026 | StatusListed |
| European Union | CE/MDR EUDAMED | Number57082653004-1SRB 05708265015337 | Date24 Feb 2026 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade Name
- Epi-Guard EUDAMEDEpiGuard GUDID
- Generic Name
- Wearable percutaneous catheter/tube holder, single-use
- Model / Reference
- 8170
- Primary DI / UDI-DI
- 05708265015337
- Basic UDI-DI
- 57082653004-1SRB
- FDA Product Code
- KGZ
- EMDN Code
- M04010299 Fixing dressings - other
- GMDN Term
- Wearable percutaneous catheter/tube holder, single-use
- Device Class
- Class I
- Regulation Number
- 878.4200
- EU market of registration
- Denmark
- GUDID distribution status
- In Commercial Distribution
Manufacturer details
- EUDAMED SRN
- CH-MF-000046832
- Authorised representative
- LiNA Medical Polska Sp. z o.o. PL-AR-000039364
Other devices from LiNA Medical AG
Properties
Other properties (17)
- 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
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Serial Number: No