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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
Pressure bandage, non-latex, reusable FDA UDI
Device Name
Supportive Elastic Athletic Wrap - 3" - Up&Up FDA UDI
Model / Reference
245-07-0426 FDA UDI
Description
Supportive Elastic Athletic Wrap - 3" - Up&Up FDA UDI

Identifiers

Primary DI / UDI-DI
00014007483001 FDA UDI
FDA Product Code
FQM FDA UDI
GMDN Term
Pressure bandage, non-latex, reusable 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

No

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Pressure bandage, non-latex, reusable

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

Similar devices

Also classified as Pressure bandage, non-latex, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Target Corporation

Sources (1)

  • FDA UDI 1c07c4fe-b82a-4348-a8d0-e66df09c1317 33 fields · synced Jun 8, 2026