← Back to catalogue
outer sheath for resectoscope 26CH rotable, perforated QL/QL
FDA UDIClass II (US FDA UDI)
Identity
- Trade Name
- outer sheath for resectoscope 26CH rotable, perforated QL/QL FDA UDI
- Generic Name
- Rigid endoscope working guide FDA UDI
- Device Name
- outer sheath for resectoscope 26CH rotable, perforated QL/QL work with 36.040.02QL/QL FDA UDI
- Model / Reference
- 36.040.01QL/QL FDA UDI
- Description
- outer sheath for resectoscope 26CH rotable, perforated QL/QL work with 36.040.02QL/QL FDA UDI
Identifiers
- Catalog Number
- 36.040.01QL/QL FDA UDI
- Primary DI / UDI-DI
- EMAH3604001QLQL0 FDA UDI
- FDA Product Code
- FDC FDA UDI
- GMDN Term
- Rigid endoscope working guide 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
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
No
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
outer sheath for resectoscope 26CH rotable, perforated QL/QL by mahe medical gmbh — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Rigid endoscope working guide.
- Strauss Surgical — AMERICAN MEDICAL ENDOSCOPY · Class II
- Strauss Surgical — AMERICAN MEDICAL ENDOSCOPY · Class II
- Olympus — Olympus Winter & Ibe GmbH · Class II
- Olympus — Olympus Winter & Ibe GmbH · Class II
- Olympus — Olympus Winter & Ibe GmbH · Class II
- Elite — Gyrus Acmi, Inc. · Class II
- Olympus — Olympus Winter & Ibe GmbH · Class II
- 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- mahe medical gmbh
Sources (1)
- FDA UDI 1c9aa378-8946-44e7-93a1-0158b32939dc 35 fields · synced Jun 1, 2026