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Rack, W/Dumbbells, 5555+5505 (2 Pc)

FDA UDI

Class I (US FDA UDI)

by Hausmann Enterprises, Llc

Identity

Trade Name
RACK,W/DUMBBELLS,5555+5505 (2 PC) FDA UDI
Generic Name
General-purpose casework FDA UDI
Model / Reference
5555-100 FDA UDI

Identifiers

Primary DI / UDI-DI
00840314806260 FDA UDI
FDA Product Code
IOD FDA UDI
GMDN Term
General-purpose casework 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: General-purpose casework

Rack, W/Dumbbells, 5555+5505 (2 Pc) by Hausmann Enterprises, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose casework.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3a49ef2a-2fbb-4fd8-a955-08d9f0b9e06c 32 fields · synced May 30, 2026