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Armedica

FDA UDI

Class I (US FDA UDI)

by Armedica Manufacturing Corp.

Identity

Trade Name
ARMEDICA FDA UDI
Generic Name
Examination/treatment table, line-powered FDA UDI
Device Name
STEEL, ELECTRIC, THREE SECTION, 27 IN WIDE TREATMENT TABLE WITH ADJUSTABLE HEAD SECTION, ADJUSTABLE FOOT SECTION, BUT WITHOUT CASTERS FDA UDI
Model / Reference
AM353 FDA UDI
Description
STEEL, ELECTRIC, THREE SECTION, 27 IN WIDE TREATMENT TABLE WITH ADJUSTABLE HEAD SECTION, ADJUSTABLE FOOT SECTION, BUT WITHOUT CASTERS FDA UDI

Identifiers

Catalog Number
AM353 FDA UDI
Primary DI / UDI-DI
B866MAM3531 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

Armedica by Armedica Manufacturing Corp. — 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 fd7d9d97-cb74-4c0f-9bd6-9cfdebd86d1d 34 fields · synced May 30, 2026