Mueller Blister Kit

FDA UDI

Class I (US FDA UDI)

by Mueller Sports Medicine, Inc.

Identity

Trade Name: Mueller Blister Kit FDA UDI
Generic Name: Wound hydrogel dressing, non-antimicrobial FDA UDI
Device Name: BLISTER KIT FDA UDI
Model / Reference: 200724 FDA UDI
Description: BLISTER KIT FDA UDI

Identifiers

Catalog Number: 200724 FDA UDI
Primary DI / UDI-DI: 00074676207247 FDA UDI
FDA Product Code: NAE FDA UDI
GMDN Term: Wound hydrogel dressing, non-antimicrobial FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4022 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

Yes

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

Yes

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

Dimensions & Sizes

Size: Length — 1.75 Inch FDA UDI
Width — 2.75 Inch FDA UDI

Category: Wound hydrogel dressing, non-antimicrobial

Mueller Blister Kit by Mueller Sports Medicine, Inc. — 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: Mueller Sports Medicine, Inc.

Sources (1)

FDA UDI a8602976-48c0-41a9-9108-f2ad7c3eb8ba 36 fields · synced Jun 9, 2026