Identity
- Trade Name
- blue endo FDA UDI
- Generic Name
- Endoscope antifog solution FDA UDI
- Device Name
- Anti fog solution alcohol free FDA UDI
- Model / Reference
- 73-000100 FDA UDI
- Description
- Anti fog solution alcohol free FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04714127863153 FDA UDI
- FDA Product Code
- OCT FDA UDI
- GMDN Term
- Endoscope antifog solution 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
Yes
FDA UDI
Single Use
Yes
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
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Endoscope antifog solution
blue endo by Unimax Medical Systems Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Endoscope antifog solution.
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- DeRoyal — DEROYAL INDUSTRIES, INC. · Class II
- ArcRoyal Anti-Fog, Regular Solution, Sterile — Aspen Surgical Products, Inc. · Class II
- Clearify — Covidien LP · Class II
- Anti-Fog w/ Pad — XODUS MEDICAL, 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 |
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Manufacturer
- Manufacturer
- Unimax Medical Systems Inc.
Sources (1)
- FDA UDI 42a71003-8d13-4efb-b5eb-fc137435af53 33 fields · synced May 31, 2026