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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
General examination/treatment chair, electric FDA UDI
Device Name
Eye Surgery Chair, Manual Base FDA UDI
Model / Reference
ESC2EYEST-MB FDA UDI
Description
Eye Surgery Chair, Manual Base FDA UDI

Identifiers

Primary DI / UDI-DI
M368ESC2EYESTMB1 FDA UDI
FDA Product Code
GBB FDA UDI
GMDN Term
General examination/treatment chair, electric 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

No

FDA UDI

Category: General examination/treatment chair, electric

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, electric.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 74feb3bf-cffa-467f-94f8-320eba8ec0d8 34 fields · synced May 31, 2026