Identity
- Trade Name
- TOMOCAP FDA UDI
- Generic Name
- Eye anterior segment analyser FDA UDI
- Model / Reference
- N/A FDA UDI
Identifiers
- Catalog Number
- 18829 FDA UDI
- Primary DI / UDI-DI
- 04059237000747 FDA UDI
- FDA Product Code
- MXK FDA UDI
- GMDN Term
- Eye anterior segment analyser FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 886.1850 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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Eye anterior segment analyser
Tomocap by Heidelberg Engineering — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- ANTERION — Heidelberg Engineering · Class II
- ANTERION — Heidelberg Engineering · Class II
- ANTERION — Heidelberg Engineering · 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
- Heidelberg Engineering
Sources (1)
- FDA UDI 631fa9f1-75fa-4c36-9bba-b2b6f54f2e1f 33 fields · synced May 30, 2026