← Back to catalogue

Hausted

FDA UDI

Class I (US FDA UDI)

by GF Health Products, Inc

Identity

Trade Name
HAUSTED FDA UDI
Generic Name
General examination/treatment chair, manual FDA UDI
Device Name
BARI PHLEB CHR W/DUAL FLIP ARM FDA UDI
Model / Reference
6200DA-VI FDA UDI
Description
BARI PHLEB CHR W/DUAL FLIP ARM FDA UDI

Identifiers

Primary DI / UDI-DI
M3686200DAVI1 FDA UDI
FDA Product Code
FML FDA UDI
GMDN Term
General examination/treatment chair, manual FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6140 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

No

FDA UDI

Category: General examination/treatment chair, manual

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

Similar devices

Also classified as General examination/treatment chair, manual.

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

Manufacturer
GF Health Products, Inc

Sources (1)

  • FDA UDI 0528c82b-4d1d-4abb-bf99-7b5d841e2f48 34 fields · synced May 31, 2026