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7', Platform Mtd, Ht&Width Adj w/Matting

FDA UDI

Class I (US FDA UDI)

by Hausmann Enterprises, Llc

Identity

Trade Name
7',Platform Mtd,Ht&Width Adj w/Matting FDA UDI
Generic Name
Parallel bar exerciser, non-powered FDA UDI
Model / Reference
1391-A68 FDA UDI

Identifiers

Primary DI / UDI-DI
00840314800268 FDA UDI
FDA Product Code
IOE FDA UDI
GMDN Term
Parallel bar exerciser, non-powered FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.5370 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Parallel bar exerciser, non-powered

7', Platform Mtd, Ht&Width Adj w/Matting by Hausmann Enterprises, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Parallel bar exerciser, non-powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b97e3d37-f6f1-4d26-baa9-7f897db49227 32 fields · synced Jun 6, 2026