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ProCure

FDA UDI

Class I (US FDA UDI)

by Twin Med, LLC

Identity

Trade Name
ProCure FDA UDI
Generic Name
Emesis bag FDA UDI
Device Name
ProCureBags, Zip Lock Clear w/White Block, 8"x10" 100ea/bag 10bg/cs FDA UDI
Model / Reference
PCBZ810 FDA UDI
Description
ProCureBags, Zip Lock Clear w/White Block, 8"x10" 100ea/bag 10bg/cs FDA UDI

Identifiers

Catalog Number
PCBZ810 FDA UDI
Primary DI / UDI-DI
10840330701423 FDA UDI
FDA Product Code
FNY FDA UDI
GMDN Term
Emesis bag FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6730 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 8 Inch FDA UDI
Width — 10 Inch FDA UDI

Category: Emesis bag

ProCure by Twin Med, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Emesis bag.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Twin Med, LLC

Sources (1)

  • FDA UDI bd7fe130-c202-494c-ab87-daf31ede1f4e 36 fields · synced May 30, 2026