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Centralite Patient Positioning Laser
FDA UDIClass I (US FDA UDI)
by Diacor Inc.
Identity
- Trade Name
- Centralite Patient Positioning Laser FDA UDI
- Generic Name
- Laser patient positioning system FDA UDI
- Device Name
- Five Moving Laser Controller w/ TPS Connectivity FDA UDI
- Model / Reference
- MLC-5PC FDA UDI
- Description
- Five Moving Laser Controller w/ TPS Connectivity FDA UDI
Identifiers
- Primary DI / UDI-DI
- B237MLC5PC0 FDA UDI
- FDA Product Code
- IWE FDA UDI
- GMDN Term
- Laser patient positioning system FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 892.5780 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
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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Centralite Patient Positioning Laser by Diacor Inc. — 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
- Diacor Inc.
Sources (1)
- FDA UDI e679ad4a-ddb4-4f4a-9714-043e527275fe 34 fields · synced Jun 6, 2026