Homann
by Aso LLC
Part of a family of 114 devices: see the family page
Ref HO-1000Model 40-3001/ 780349 / 40-3003 / 780351 / 40-3014 / 752825 / 40-3070 / 2003043 / 40-3071 / 2003041 / 40-3075 / 2003042 / 40-4013 / 752892 / 40-6001 / 781429 / 40-6003 / 781430 / 40-6013 / 781431 / 75-1623 / 781623 / 75-4331 / 754331 / 75-4378 / 754378
Homann (HO-1000) is a Class IIa device made by Aso LLC, registered in EUDAMED on 31 Jan 2024 (Basic UDI-DI 0017276M226M3), withdrawn as of 25 Oct 2026.
Withdrawn
CE MDR, withdrawn
Ended
Withdrawn
FDA recalls
Not applicable
Documents
None linked in EUDAMED
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number0017276M226M3 04101230011302 | Date31 Jan 2024 | StatusWithdrawn |
Official records
- EUDAMED public site 0017276M226M3
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Withdrawn
Specification
- Device name
- Non-Sterile Hydrocolloid Bandages
- Model / reference
- 40-3001/ 780349 / 40-3003 / 780351 / 40-3014 / 752825 / 40-3070 / 2003043 / 40-3071 / 2003041 / 40-3075 / 2003042 / 40-4013 / 752892 / 40-6001 / 781429 / 40-6003 / 781430 / 40-6013 / 781431 / 75-1623 / 781623 / 75-4331 / 754331 / 75-4378 / 754378, HO-1000
- Primary DI / UDI-DI
- 04101230011302
- Basic UDI-DI
- 0017276M226M3
- EMDN code
- M04040301 Hydrocolloid dressings, non-combined
- Device class
- Class IIa
- EU registration type
- Standard device
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- US-MF-000008641
- Authorised representative
- Aso Europe BV NL-AR-000004377
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