Identity
- Trade Name
- Ritter FDA UDI
- Generic Name
- Fixed examination/treatment room light FDA UDI
- Device Name
- The Ritter Mobile (without power cord) LED Procedure Light is intended to be used in medical environments where illumination is required for medical use during external examinations and procedures. FDA UDI
- Model / Reference
- 255-007 FDA UDI
- Description
- The Ritter Mobile (without power cord) LED Procedure Light is intended to be used in medical environments where illumination is required for medical use during external examinations and procedures. FDA UDI
Identifiers
- Catalog Number
- 255-007 FDA UDI
- Primary DI / UDI-DI
- 00841709106798 FDA UDI
- FDA Product Code
- KZF FDA UDI
- GMDN Term
- Fixed examination/treatment room light FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.6320 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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Fixed examination/treatment room light
Ritter by Midmark Corporation — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- Midmark Corporation
Sources (1)
- FDA UDI 7a615ecf-2f53-4963-b9ac-4a7508beb6a3 36 fields · synced Jun 8, 2026