← Back to catalogue
innner sheath 5Ch.channel for 2.9mm/30° telescopes
FDA UDIClass II (US FDA UDI)
Identity
- Trade Name
- innner sheath 5Ch.channel for 2.9mm/30° telescopes FDA UDI
- Generic Name
- Rigid endoscope telescope FDA UDI
- Device Name
- innner sheath 5Ch.channel for 2.9mm/30° telescopes FDA UDI
- Model / Reference
- 30.019.051QL FDA UDI
- Description
- innner sheath 5Ch.channel for 2.9mm/30° telescopes FDA UDI
Identifiers
- Catalog Number
- 30.019.051QL FDA UDI
- Primary DI / UDI-DI
- EMAH30019051QL0 FDA UDI
- FDA Product Code
- HET FDA UDI
- GMDN Term
- Rigid endoscope telescope FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 884.1720 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 telescope
innner sheath 5Ch.channel for 2.9mm/30° telescopes by mahe medical gmbh — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Rigid endoscope telescope.
- Medline — MEDLINE INDUSTRIES, INC. · Class II
- Olympus — Olympus Winter & Ibe GmbH · Class II
- ELMED — ELMED INCORPORATED · Class II
- ELMED — ELMED INCORPORATED · Class I
- Olympus — Olympus Winter & Ibe GmbH · Class II
- PANOVIEW PLUS HD — Richard Wolf GmbH · Class II
- PANOVIEW PLUS — Richard Wolf GmbH · Class II
- Millennium — AVALIGN TECHNOLOGIES, Inc. · Class I
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 f482c8de-6974-4cbb-bb56-4282c4455c3d 35 fields · synced May 31, 2026