Identity
- Trade Name
- zumax FDA UDI
- Generic Name
- Retinoscope, line-powered FDA UDI
- Device Name
- Desk-top streak retinoscope FDA UDI
- Model / Reference
- SR24F FDA UDI
- Description
- Desk-top streak retinoscope FDA UDI
Identifiers
- Primary DI / UDI-DI
- 06945095531203 FDA UDI
- FDA Product Code
- HKL FDA UDI
- GMDN Term
- Retinoscope, line-powered FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 886.1780 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
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Retinoscope, line-powered
zumax by Zumax Medical Co., LTD — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Zumax Medical Co., LTD
Sources (1)
- FDA UDI 16cd28e1-9b96-46cf-9e9f-c04554c34c35 33 fields · synced May 30, 2026