Identity
- Trade Name
- Domia Front FDA UDI
- Generic Name
- Urinary stone retrieval basket, single-use FDA UDI
- Device Name
- Dormia 2Fr 8mm Stone Extractor FDA UDI
- Model / Reference
- DOF208 FDA UDI
- Description
- Dormia 2Fr 8mm Stone Extractor FDA UDI
Identifiers
- Catalog Number
- DOF208 FDA UDI
- Primary DI / UDI-DI
- B937DOF2080 FDA UDI
- FDA Product Code
- FFL FDA UDI
- GMDN Term
- Urinary stone retrieval basket, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.4680 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
MR Unsafe FDA UDI
Category: Urinary stone retrieval basket, single-use
Domia Front by EPflex Feinwerktechnik GmbH. — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
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Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Unknown
MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | MDR | — | Class II | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- EPflex Feinwerktechnik GmbH.
Sources (2)
- FDA UDI be40b4bd-f8a5-48ad-b536-1ddc6f0b63ec 34 fields · synced Jun 18, 2026
- EUDAMED 1 fields · synced Jun 3, 2026