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5556+wt, (2)5503, (2)5588, 5541(6 Pc)

FDA UDI

Class I (US FDA UDI)

by Hausmann Enterprises, Llc

Identity

Trade Name
5556+WT,(2)5503,(2)5588,5541(6 PC) FDA UDI
Generic Name
General-purpose casework FDA UDI
Model / Reference
5556-100 FDA UDI

Identifiers

Primary DI / UDI-DI
00840314806277 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

5556+wt, (2)5503, (2)5588, 5541(6 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 e5a82af6-9a41-4fd1-ac50-d3b628f113f9 32 fields · synced Jun 8, 2026