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Bt-Da22-Ia
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref BT-DMF-003Model BT-DA24-IA, BT-DB24-IA, BT-DA22-IA, BT-DB22-IA, BT-DA22W, BT-DB22W
Identity
- Trade Name
- BT-DA22-IA EUDAMEDBSD3543 Digital Flat Panel X-ray Detector FDA UDI
- Generic Name
- Indirect flat panel x-ray detector FDA UDI
- Model / Reference
- BT-DA24-IA, BT-DB24-IA, BT-DA22-IA, BT-DB22-IA, BT-DA22W, BT-DB22W EUDAMEDBT-DMF-003 EUDAMEDBT-DA22-IA FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08800069500013 EUDAMEDFDA UDI
- Basic UDI-DI
- 880006950CG2422WWV EUDAMED
- Direct Marketing DI
- 08800069500013 EUDAMED
- FDA Product Code
- MQB FDA UDI
- EMDN Code
- Z11030599 RADIOLOGY INSTRUMENTS - OTHER EUDAMED
- GMDN Term
- Indirect flat panel x-ray detector FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass II FDA UDI
- Regulation Number
- 892.1680 FDA UDI
- Market of Registration
- Poland EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
Yes
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Bt-Da22-Ia by BONTECH Co., Ltd. — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 880006950CG2422WWV | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
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Manufacturer
- Manufacturer
- BONTECH Co., Ltd.
- EUDAMED SRN
- KR-MF-000048185
- Authorised Representative
- CMC Medical Devices & Drugs SL ES-AR-000000293
Sources (2)
- EUDAMED d3be16df-63a4-44b8-9774-a7188c385f5f 61 fields · synced Jun 18, 2026
- FDA UDI f452861a-de29-4ddc-b1e8-1fe8a157f03d 32 fields · synced May 30, 2026