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Medline

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline FDA UDI
Generic Name
Skin treatment/dressing-supportive limb/finger bandage, single-use FDA UDI
Device Name
DBD-BANDAGE,SRTSTRTCH,10CMX5M,3.94X5.47Y FDA UDI
Model / Reference
MDS099004SSHL FDA UDI
Description
DBD-BANDAGE,SRTSTRTCH,10CMX5M,3.94X5.47Y FDA UDI

Identifiers

Catalog Number
MDS099004SSHL FDA UDI
Primary DI / UDI-DI
10888277702288 FDA UDI
FDA Product Code
FQM FDA UDI
GMDN Term
Skin treatment/dressing-supportive limb/finger bandage, 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

Yes

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: Skin treatment/dressing-supportive limb/finger bandage, single-use

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

Similar devices

Also classified as Skin treatment/dressing-supportive limb/finger bandage, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medline Industries, Inc.

Sources (1)

  • FDA UDI 20f13528-7c8d-46a3-b85d-4ff75c4ccc16 35 fields · synced Jun 8, 2026