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UMF Medical

FDA UDI

Class I (US FDA UDI)

by United Metal Fabricators, Inc.

Identity

Trade Name
UMF Medical FDA UDI
Generic Name
Examination/treatment table, line-powered FDA UDI
Device Name
4010-650 HEAD CENTRIC PROCEDURE CHAIR- HC/FC- FIRE RATED UPHOLSTERY FDA UDI
Model / Reference
4010-650-200F FDA UDI
Description
4010-650 HEAD CENTRIC PROCEDURE CHAIR- HC/FC- FIRE RATED UPHOLSTERY FDA UDI

Identifiers

Primary DI / UDI-DI
00815235020682 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
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

No

FDA UDI

UMF Medical by United Metal Fabricators, 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

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Manufacturer

Sources (1)

  • FDA UDI 373d2b0a-9be9-4e48-b3ae-146c2bb3094f 34 fields · synced Jun 6, 2026