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Kbmed

FDA UDI

Class I (US FDA UDI)

by KB Medical (group), Inc.

Identity

Trade Name
KBMED FDA UDI
Generic Name
Non-adhesive device retention bandage FDA UDI
Device Name
Cohesive Bandage, Tan, 1"x 5 yard, pack of 60 rolls FDA UDI
Model / Reference
SCB1050 FDA UDI
Description
Cohesive Bandage, Tan, 1"x 5 yard, pack of 60 rolls FDA UDI

Identifiers

Primary DI / UDI-DI
10810100051270 FDA UDI
FDA Product Code
FQM FDA UDI
KGX FDA UDI
GMDN Term
Non-adhesive device retention bandage FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5075 FDA UDI
880.5240 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Non-adhesive device retention bandage

Kbmed by KB Medical (group), Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Non-adhesive device retention bandage.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
KB Medical (group), Inc.

Sources (1)

  • FDA UDI cb9314ae-af11-44b5-964e-3c69ea6750ef 33 fields · synced Jun 8, 2026