Identity
- Trade Name
- mahe medical GmbH FDA UDI
- Generic Name
- Footrest FDA UDI
- Device Name
- Lithotripsy Telescope bridge w.7Ch. _x000D_working channel _x000D_ FDA UDI
- Model / Reference
- 35.009.15QL FDA UDI
- Description
- Lithotripsy Telescope bridge w.7Ch. _x000D_working channel _x000D_ FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04050659368828 FDA UDI
- FDA Product Code
- JFL FDA UDI
- GMDN Term
- Footrest FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 862.1160 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Footrest
mahe medical GmbH by mahe medical gmbh — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- mahe medical gmbh
Sources (1)
- FDA UDI 4f104d0b-049e-4bf0-8120-42fc71dfae0f 33 fields · synced Jun 1, 2026