Dansac
by Hollister Incorporated 2 variants
Ref 897-00, 12102-102
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 | Number610075D02P022S023786 | Date23 Apr 2025 | 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- Withdrawn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
- 1-Piece Post-Op Ostomy Pouch, GX+, High Output, Sterile2-Piece Post-Op Ostomy Set, GX+, High Output, Sterile
- Model / Reference
- 897-00, 12102-102
- Primary DI / UDI-DI
- 05709817530308, 05709817406078
- Basic UDI-DI
- 610075D02P022S023786, 610075D02P086S0240CM
- Unit of Use DI
- 25709817530302, 25709817406072
- EMDN Code
- A1001020102, A100299
- Device Class
- Class I
- EU market of registration
- Ireland
Manufacturer details
- EUDAMED SRN
- US-MF-000027818
- Authorised representative
- Hollister ULC IE-AR-000022119
Other devices from Hollister Incorporated
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