Identity
- Trade Name
- LIFETEC FDA UDI
- Generic Name
- Examination/treatment table, line-powered FDA UDI
- Device Name
- STEEL, ELECTRIC, BAR ACTIVATED, TWO SECTION, 40 IN WIDE TREATMENT TABLE WITH ADJUSTABLE HEAD SECTION, SIDE PANELS, AND CASTERS FDA UDI
- Model / Reference
- LAMBA240 FDA UDI
- Description
- STEEL, ELECTRIC, BAR ACTIVATED, TWO SECTION, 40 IN WIDE TREATMENT TABLE WITH ADJUSTABLE HEAD SECTION, SIDE PANELS, AND CASTERS FDA UDI
Identifiers
- Catalog Number
- LAMBA240 FDA UDI
- Primary DI / UDI-DI
- B866MLAMBA2401 FDA UDI
- FDA Product Code
- INQ FDA UDI
- GMDN Term
- Examination/treatment table, line-powered FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 890.3760 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
No
FDA UDI
Category: Examination/treatment table, line-powered
Lifetec by Armedica Manufacturing Corp. — 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
- Armedica Manufacturing Corp.
Sources (1)
- FDA UDI 0841774f-dc28-44f9-823d-f3afa91a8f17 34 fields · synced May 30, 2026