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The Emergency Elastic Wrap

FDA UDI

Class I (US FDA UDI)

by Einstein Works, Llc

Identity

Trade Name
THE EMERGENCY ELASTIC WRAP FDA UDI
Generic Name
Pressure bandage, non-latex, single-use FDA UDI
Device Name
THE EMERGENCY ELASTIC WRAP - 4" FDA UDI
Model / Reference
1 FDA UDI
Description
THE EMERGENCY ELASTIC WRAP - 4" FDA UDI

Identifiers

Primary DI / UDI-DI
00860017001298 FDA UDI
FDA Product Code
FQM FDA UDI
GMDN Term
Pressure 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

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Pressure bandage, non-latex, single-use

The Emergency Elastic Wrap by Einstein Works, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pressure bandage, non-latex, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Einstein Works, Llc

Sources (1)

  • FDA UDI 7e49c9fa-0e80-4cc3-97b7-ec15c536c9d0 33 fields · synced May 30, 2026