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Medline

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline FDA UDI
Generic Name
Skin-approximation adhesive FDA UDI
Device Name
SKIN AFFIX SURG ADHESIVE 72/CS 0.55ML FDA UDI
Model / Reference
MSC091040 FDA UDI
Description
SKIN AFFIX SURG ADHESIVE 72/CS 0.55ML FDA UDI

Identifiers

Catalog Number
MSC091040 FDA UDI
Primary DI / UDI-DI
10884389953044 FDA UDI
510(k) Number
K132243 FDA UDI
FDA Product Code
MPN FDA UDI
GMDN Term
Skin-approximation adhesive FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4010 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Skin-approximation adhesive

Medline by Medline Industries, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Skin-approximation adhesive.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0167709e-fa3d-4432-b597-2ce64a5760b7 36 fields · synced May 30, 2026