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Medline

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline FDA UDI
Generic Name
Multi-purpose surgical skin adhesive tape FDA UDI
Device Name
BNDG,ELSTC,MATRIX,STRL,3"X5YD,LF,HOOK&LP FDA UDI
Model / Reference
DYNJ05153LF FDA UDI
Description
BNDG,ELSTC,MATRIX,STRL,3"X5YD,LF,HOOK&LP FDA UDI

Identifiers

Catalog Number
DYNJ05153LF FDA UDI
Primary DI / UDI-DI
10080196823505 FDA UDI
FDA Product Code
FQM FDA UDI
GMDN Term
Multi-purpose surgical skin adhesive tape FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5075 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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Multi-purpose surgical skin adhesive tape

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

Similar devices

Also classified as Multi-purpose surgical skin adhesive tape.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 60514691-ac79-4390-bfae-e7a3ae48b8bb 35 fields · synced May 30, 2026