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Hausted

FDA UDI

Class I (US FDA UDI)

by GF Health Products, Inc

Identity

Trade Name
HAUSTED FDA UDI
Generic Name
Examination/treatment table, manual FDA UDI
Device Name
EXAM TABLE W/DRAWERS, STIRRUPS FDA UDI
Model / Reference
4200-TE FDA UDI
Description
EXAM TABLE W/DRAWERS, STIRRUPS FDA UDI

Identifiers

Primary DI / UDI-DI
M3684200TE1 FDA UDI
FDA Product Code
LGX FDA UDI
GMDN Term
Examination/treatment table, manual FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4960 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Examination/treatment table, manual

Hausted by GF Health Products, Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Examination/treatment table, manual.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI eae846ad-4dc0-4c6c-ba10-7015ef0430e4 34 fields · synced Jun 8, 2026