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meijer

FDA UDI

Class I (US FDA UDI)

by Meijer, Inc.

Identity

Trade Name
meijer FDA UDI
Generic Name
Exudate-absorbent dressing, hydrophilic-gel, non-sterile FDA UDI
Device Name
Extreme Hydrocolloid blister cushion, all one size, 42 mm x 68 mm FDA UDI
Model / Reference
713733229203 FDA UDI
Description
Extreme Hydrocolloid blister cushion, all one size, 42 mm x 68 mm FDA UDI

Identifiers

Catalog Number
4300495 FDA UDI
Primary DI / UDI-DI
00713733229203 FDA UDI
FDA Product Code
NAD FDA UDI
GMDN Term
Exudate-absorbent dressing, hydrophilic-gel, non-sterile FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4020 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Exudate-absorbent dressing, hydrophilic-gel, non-sterile

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

Similar devices

Also classified as Exudate-absorbent dressing, hydrophilic-gel, non-sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Meijer, Inc.

Sources (1)

  • FDA UDI d0d02249-d1d3-4825-a394-82f1acef7027 34 fields · synced May 30, 2026