← Back to catalogue

Pneumex

FDA UDI

Class I (US FDA UDI)

by Armedica Manufacturing Corp.

Identity

Trade Name
PNEUMEX FDA UDI
Generic Name
Examination/treatment table, line-powered FDA UDI
Device Name
STEEL, ELECTRIC, BAR ACTIVATED, 600 LB RATED, MULTI SECTION TREATMENT TABLE WITH VIBRATION FDA UDI
Model / Reference
PNEBA100 FDA UDI
Description
STEEL, ELECTRIC, BAR ACTIVATED, 600 LB RATED, MULTI SECTION TREATMENT TABLE WITH VIBRATION FDA UDI

Identifiers

Catalog Number
PNEBA100 FDA UDI
Primary DI / UDI-DI
B866MPNEBA1001 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

Pneumex 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 70fd1647-f174-455a-8283-66e429eb53c3 34 fields · synced Jun 8, 2026