Meijer

FDA UDI

Class I (US FDA UDI)

by Meijer, Inc.

Identity

Trade Name: MEIJER FDA UDI
Generic Name: Dressing-fixation skin adhesive tape, silicone FDA UDI
Device Name: MEIJER SILICONE TAPE FDA UDI
Model / Reference: 4705080 FDA UDI
Description: MEIJER SILICONE TAPE FDA UDI

Identifiers

Primary DI / UDI-DI: 00760236206811 FDA UDI
FDA Product Code: HXT FDA UDI
GMDN Term: Dressing-fixation skin adhesive tape, silicone FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4800 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Dressing-fixation skin adhesive tape, silicone

Meijer by Meijer, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dressing-fixation skin adhesive tape, silicone.

ComfiTape — DERMARITE INDUSTRIES LLC · Class I
Acanthus — ACANTHUS MEDICAL CREATIONS, LLC · Class I
Hydrogel Adhesive — VivaLNK, Inc. · Class I
Silicone Bandage — AP MDS Co., Ltd. · Class I
McKesson — MCKESSON MEDICAL-SURGICAL INC. · Class I
FifthPulse — Jeg & Sons Inc. · Class I
OFFSET MODULAR HEAD PROVISIONAL — Biomet Orthopedics, Inc. · Class I
Acanthus — ACANTHUS MEDICAL CREATIONS, LLC · Class I

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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: Meijer, Inc.

Sources (1)

FDA UDI bcaf9003-6385-41e8-b934-2cac5403c96a 33 fields · synced May 30, 2026