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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
General-purpose patient lifting system sling/harness FDA UDI
Device Name
KNEE STRAP FOR LF2020, LF2090 FDA UDI
Model / Reference
SAL1230-KB FDA UDI
Description
KNEE STRAP FOR LF2020, LF2090 FDA UDI

Identifiers

Catalog Number
SAL1230-KB FDA UDI
Primary DI / UDI-DI
M368SAL1230KB1 FDA UDI
FDA Product Code
FSA FDA UDI
GMDN Term
General-purpose patient lifting system sling/harness FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5510 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

Yes

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 patient lifting system sling/harness

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

Similar devices

Also classified as General-purpose patient lifting system sling/harness.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
GF Health Products, Inc

Sources (1)

  • FDA UDI 42c5bb1e-0a5e-4262-b33d-0e96b39f9e41 35 fields · synced May 31, 2026