Identity
- Trade Name
- mahe medical GmbH FDA UDI
- Generic Name
- Resectoscope FDA UDI
- Device Name
- Uretero-Renoscope,425mm,rigid,distal end_x000D_6/7.5Ch., work.channel 4Ch. _x000D_direct.of view 8° to working channel FDA UDI
- Model / Reference
- 35.003.06 FDA UDI
- Description
- Uretero-Renoscope,425mm,rigid,distal end_x000D_6/7.5Ch., work.channel 4Ch. _x000D_direct.of view 8° to working channel FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04050659367746 FDA UDI
- FDA Product Code
- GCJ FDA UDI
- GMDN Term
- Resectoscope FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.1500 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: Resectoscope
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 581be1f4-5a45-44a5-885a-2847e06170e6 33 fields · synced Jun 8, 2026