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Upper Cervical Store

FDA UDI

Class I (US FDA UDI)

by Upper Cervical Store Inc

Identity

Trade Name
Upper Cervical Store FDA UDI
Generic Name
Examination/treatment table, line-powered FDA UDI
Device Name
Elevating Table FDA UDI
Model / Reference
ET FDA UDI
Description
Elevating Table FDA UDI

Identifiers

Primary DI / UDI-DI
00628942541605 FDA UDI
FDA Product Code
INW FDA UDI
GMDN Term
Examination/treatment table, line-powered FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3750 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

Upper Cervical Store by Upper Cervical Store Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Examination/treatment table, line-powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI de01a3bf-e72c-4b68-ba33-973a9a35e96b 33 fields · synced May 31, 2026