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Lumex

FDA UDI

Class I (US FDA UDI)

by GF Health Products, Inc

Identity

Trade Name
Lumex FDA UDI
Generic Name
Reclining chair FDA UDI
Device Name
RECL DR ARM HEAT&MAS SLV TAUPE FDA UDI
Model / Reference
FR566DGH8809 FDA UDI
Description
RECL DR ARM HEAT&MAS SLV TAUPE FDA UDI

Identifiers

Catalog Number
FR566DGH8809 FDA UDI
Primary DI / UDI-DI
M368FR566DGH88091 FDA UDI
FDA Product Code
INM FDA UDI
GMDN Term
Reclining chair FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3100 FDA UDI
Commercial Distribution
Not 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

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e75d4285-398c-474a-87cd-1ebcda48d032 36 fields · synced Jun 1, 2026