Identity
- Trade Name
- Resectoscopy obturator only,26Ch. FDA UDI
- Generic Name
- Rigid endoscope working guide FDA UDI
- Device Name
- Resectoscopy obturator only,26Ch. FDA UDI
- Model / Reference
- 36.006.03 FDA UDI
- Description
- Resectoscopy obturator only,26Ch. FDA UDI
Identifiers
- Catalog Number
- 36.006.03 FDA UDI
- Primary DI / UDI-DI
- EMAH36006030 FDA UDI
- FDA Product Code
- JFL FDA UDI
- GMDN Term
- Rigid endoscope working guide 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
No
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
Yes
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Rigid endoscope working guide
Resectoscopy obturator only, 26Ch. by mahe medical gmbh — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- USA Elite — Gyrus Acmi, Inc. · Class II
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 146afe55-ef1e-4c34-978f-7f8cc48bc3d5 35 fields · synced May 30, 2026