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Medline

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline FDA UDI
Generic Name
Tubular support bandage, non-latex, single-use FDA UDI
Device Name
BNDG,TUBLR,MEDIGRIP SZ A 1-3/4W,LF FDA UDI
Model / Reference
MSC9500LF FDA UDI
Description
BNDG,TUBLR,MEDIGRIP SZ A 1-3/4W,LF FDA UDI

Identifiers

Catalog Number
MSC9500LF FDA UDI
Primary DI / UDI-DI
10888277718593 FDA UDI
FDA Product Code
MHW FDA UDI
GMDN Term
Tubular support bandage, non-latex, single-use 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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Tubular support bandage, non-latex, single-use

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

Similar devices

Also classified as Tubular support bandage, non-latex, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7d812185-559e-4ad1-9767-a793e7dd6729 35 fields · synced Jun 1, 2026