Identity
- Trade Name
- MOPTIM FDA UDI
- Generic Name
- Ophthalmic surgical microscope FDA UDI
- Device Name
- The operating microscope refers to a compound micro-magnification device composed of cold light source, objective lens, eyepiece, optical zoom system and bracket. Operating microscope can generally be divided into three parts: mechanical systems, observation systems, and lighting systems. Vertical operating microscopes (floor-mounted) are generally used for ophthalmic surgery. The feature of this type of operating microscope is that it can be placed arbitrarily, and is more flexible and easy to install. FDA UDI
- Model / Reference
- OPM500 FDA UDI
- Description
- The operating microscope refers to a compound micro-magnification device composed of cold light source, objective lens, eyepiece, optical zoom system and bracket. Operating microscope can generally be divided into three parts: mechanical systems, observation systems, and lighting systems. Vertical operating microscopes (floor-mounted) are generally used for ophthalmic surgery. The feature of this type of operating microscope is that it can be placed arbitrarily, and is more flexible and easy to install. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 06972039971221 FDA UDI
- FDA Product Code
- HRM FDA UDI
- GMDN Term
- Ophthalmic surgical microscope FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4700 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
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Ophthalmic surgical microscope
Moptim by Shenzhen CERTAINN Technology Co., Ltd. — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- Shenzhen CERTAINN Technology Co., Ltd.
Sources (1)
- FDA UDI 5d5de69b-9cb9-406c-bbb6-0e28265df2d1 33 fields · synced May 31, 2026