Identity
- Trade Name
- ATLAS Corneal Topography System FDA UDI
- Generic Name
- Corneal topography system FDA UDI
- Device Name
- The ZEISS ATLAS Corneal Topography System is intended to measure and analyze the corneal curvature of the eye. FDA UDI
- Model / Reference
- 9000 FDA UDI
- Description
- The ZEISS ATLAS Corneal Topography System is intended to measure and analyze the corneal curvature of the eye. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04057748081118 FDA UDI
- FDA Product Code
- HJB FDA UDI
- GMDN Term
- Corneal topography system FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 886.1450 FDA UDI
- Commercial Distribution
- Not 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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
ATLAS Corneal Topography System by Carl Zeiss Meditec AG — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Carl Zeiss Meditec AG
Sources (1)
- FDA UDI f63ad62f-68b5-4002-b5a4-1cf3055ff848 34 fields · synced Jun 1, 2026