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Up&Up

FDA UDI

Class I (US FDA UDI)

by Target Corporation

Identity

Trade Name
Up&Up FDA UDI
Generic Name
Skin-cover adhesive strip, non-antimicrobial FDA UDI
Device Name
Flexible Fabric Extra Large Bandages, 2 IN x 4 IN (5 cm x 10.1 cm) FDA UDI
Model / Reference
245070727 FDA UDI
Description
Flexible Fabric Extra Large Bandages, 2 IN x 4 IN (5 cm x 10.1 cm) FDA UDI

Identifiers

Primary DI / UDI-DI
00017276226256 FDA UDI
FDA Product Code
KGX FDA UDI
GMDN Term
Skin-cover adhesive strip, non-antimicrobial FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5240 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

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-cover adhesive strip, non-antimicrobial

Up&Up by Target Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Skin-cover adhesive strip, non-antimicrobial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Target Corporation

Sources (1)

  • FDA UDI fa40e9cf-4dd5-4097-9b29-ed68f0d6af30 34 fields · synced Jun 8, 2026