Identity
- Device Name
- Biopsy Forceps EUDAMED
- Model / Reference
- HQ1.8 EUDAMEDHQ-1.8×1050-W-O EUDAMED
Identifiers
- Primary DI / UDI-DI
- 06941173337422 EUDAMED
- Basic UDI-DI
- B-06941173337422 EUDAMED
- EMDN Code
- K01020104 MINIMALLY INVASIVE SURGERY FORCEPS, SINGLE-USE EUDAMED
Classification
- Device Class
- Class IIa EUDAMED
- Market of Registration
- Austria EUDAMED
Clinical & Handling
Sterile
Yes
EUDAMED
Implantable
No
EUDAMED
Reusable
No
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Biopsy Forceps by Jiangsu BANA Medical Technology Co., Ltd. — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDD
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-06941173337422 | Class IIa | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Jiangsu BANA Medical Technology Co., Ltd.
- EUDAMED SRN
- CN-MF-000025963
- Authorised Representative
- Caretechion GmbH DE-AR-000005946
Sources (1)
- EUDAMED db3db691-5240-42ca-ab07-473d316ca2c4 61 fields · synced Jun 11, 2026