Labotek Spot Bandage

FDA UDI

Class I (US FDA UDI)

by Labotek Group Corp

Identity

Trade Name: Labotek Spot Bandage FDA UDI
Generic Name: Adhesive bandage FDA UDI
Device Name: Labotek Spot Bandage, 25 mm overall size, Ventilated, Individually wrapped FDA UDI
Model / Reference: RR-150 FDA UDI
Description: Labotek Spot Bandage, 25 mm overall size, Ventilated, Individually wrapped FDA UDI

Identifiers

Primary DI / UDI-DI: 00850014448158 FDA UDI
FDA Product Code: KGX FDA UDI
GMDN Term: Adhesive bandage FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 880.5240 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

Yes

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Adhesive bandage

Labotek Spot Bandage by Labotek Group Corp — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Labotek Group Corp

Sources (1)

FDA UDI 0c65ed52-81b4-4eca-a2d1-7e196b6b342a 34 fields · synced May 30, 2026