Identity
- Trade Name
- Procedure Chair FDA UDI
- Generic Name
- Examination/treatment table, line-powered FDA UDI
- Device Name
- 3 Section Top; 27" Width; 120V Electric FDA UDI
- Model / Reference
- 100 Procedure Chair / PCG Chair FDA UDI
- Description
- 3 Section Top; 27" Width; 120V Electric FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00817463026641 FDA UDI
- FDA Product Code
- LGX FDA UDI
- GMDN Term
- Examination/treatment table, line-powered FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4960 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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Procedure Chair by Oakworks, 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
- Oakworks, Inc.
Sources (1)
- FDA UDI 2243cc6d-92bf-4c92-9c48-1a3000702f65 34 fields · synced Jun 7, 2026