Identity
- Trade Name
- HEINE BETA® 200 S LED Diagnostic Set FDA UDI
- Generic Name
- Direct ophthalmoscope FDA UDI
- Model / Reference
- S FDA UDI
Identifiers
- Catalog Number
- C-248.25.487 FDA UDI
- Primary DI / UDI-DI
- 04053755188543 FDA UDI
- FDA Product Code
- HLJ FDA UDI
- GMDN Term
- Direct ophthalmoscope FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 886.1570 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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Direct ophthalmoscope
HEINE BETA® 200 S LED Diagnostic Set by Heine Optotechnik GmbH & Co. KG — 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
- Heine Optotechnik GmbH & Co. KG
Sources (1)
- FDA UDI 778fff3b-449b-4232-8318-5cd40e9c1288 34 fields · synced May 30, 2026