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Mestopore®

FDA UDI

Class I (US FDA UDI)

by Mölnlycke Health Care AB

Identity

Trade Name
Mestopore® FDA UDI
Generic Name
Absorbent stomal dressing FDA UDI
Device Name
Mestopore FDA UDI
Model / Reference
665000 FDA UDI
Description
Mestopore FDA UDI

Identifiers

Primary DI / UDI-DI
07323190242757 FDA UDI
FDA Product Code
NAC FDA UDI
GMDN Term
Absorbent stomal dressing FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4018 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

No

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: Absorbent stomal dressing

Mestopore® by Mölnlycke Health Care AB — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Absorbent stomal dressing.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Mölnlycke Health Care AB

Sources (1)

  • FDA UDI 9f45cace-c1aa-409c-b362-e83673b53f5c 35 fields · synced May 30, 2026