← Back to catalogue

Work Hardening Intermediate Package

FDA UDI

Class I (US FDA UDI)

by Hausmann Enterprises, Llc

Identity

Trade Name
WORK HARDENING INTERMEDIATE PACKAGE FDA UDI
Generic Name
Chest-press exerciser FDA UDI
Model / Reference
SYSTEM-II FDA UDI

Identifiers

Primary DI / UDI-DI
00840314806482 FDA UDI
FDA Product Code
IOD FDA UDI
GMDN Term
Chest-press exerciser FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.5350 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: Chest-press exerciser

Work Hardening Intermediate Package by Hausmann Enterprises, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Chest-press exerciser.

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 eb788c2e-7f49-4f49-965a-b76075ccb331 32 fields · synced May 30, 2026