Identity
- Trade Name
- MITEK FDA UDI
- Generic Name
- Rigid optical arthroscope, reusable FDA UDI
- Device Name
- HD EP Arthroscope/Sinuscope compatible with Mitek Lock 4.0mm x 30 deg x 270mm FDA UDI
- Model / Reference
- 242022 FDA UDI
- Description
- HD EP Arthroscope/Sinuscope compatible with Mitek Lock 4.0mm x 30 deg x 270mm FDA UDI
Identifiers
- Catalog Number
- 242022 FDA UDI
- Primary DI / UDI-DI
- 10886705028979 FDA UDI
- FDA Product Code
- HRX FDA UDIEOB FDA UDI
- GMDN Term
- Rigid optical arthroscope, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.1100 FDA UDI874.4760 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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Rigid optical arthroscope, reusable
Mitek by Medos International Sàrl — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Rigid optical arthroscope, reusable.
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- AED — NATIONAL ADVANCED ENDOSCOPY DEVICES, INC. · Class II
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- HOPKINS — Karl Storz GmbH & Co. KG · Class II
- Olympus — Olympus Winter & Ibe GmbH · Class II
- Surgical Direct — SURGICAL DIRECT, INC. · Class II
- HOPKINS — Karl Storz GmbH & Co. KG · Class II
- Precision Ideal Eyes — Stryker Corp. · Class II
Cleared under the same submission
K080560 also covers:
- MITEK — Medos International Sàrl
- MITEK — Medos International Sàrl
- MITEK — Medos International Sàrl
- MITEK — Medos International Sàrl
- MITEK — Medos International Sàrl
- MicroAire® — MicroAire Surgical Instruments LLC
- MicroAire® — MicroAire Surgical Instruments LLC
- IRIS Arthroscope — SOLENDOS Inc.
- IRIS Arthroscope — SOLENDOS Inc.
- IRIS Arthroscope — SOLENDOS Inc.
- IRIS Arthroscope — SOLENDOS Inc.
- IRIS Arthroscope — SOLENDOS Inc.
K981751 also covers:
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
- Medos International Sàrl
Sources (1)
- FDA UDI 3ec7db5d-19a6-40dc-b73d-a265e4da9d7a 36 fields · synced May 30, 2026