Hook Lock™

FDA UDI

Class I (US FDA UDI)

by Tetra Medical Supply Corp.

Identity

Trade Name: HOOK LOCK™ FDA UDI
Generic Name: Pressure bandage, non-latex, single-use FDA UDI
Device Name: STERILE HOOK LOCK LATEX FREE ELASTIC BANDAGE 3INX5YD FDA UDI
Model / Reference: 6611-3S FDA UDI
Description: STERILE HOOK LOCK LATEX FREE ELASTIC BANDAGE 3INX5YD FDA UDI

Identifiers

Catalog Number: 6611-3S FDA UDI
Primary DI / UDI-DI: 00614138122291 FDA UDI
FDA Product Code: FQM FDA UDI
GMDN Term: Pressure bandage, non-latex, single-use FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 880.5075 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

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

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Ethylene Oxide FDA UDI

Category: Pressure bandage, non-latex, single-use

Hook Lock™ by Tetra Medical Supply 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: Tetra Medical Supply Corp.

Sources (1)

FDA UDI 1d107665-6f0d-4012-becb-097d83a2ba87 35 fields · synced May 30, 2026