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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 9"x12" - 100/bg 10bg/cs FDA UDI
Model / Reference
PCBZ912 FDA UDI
Description
ProCureBags Zip Lock Clear 9"x12" - 100/bg 10bg/cs FDA UDI

Identifiers

Catalog Number
PCBZ912 FDA UDI
Primary DI / UDI-DI
10840330701430 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 — 9 Inch FDA UDI
Width — 12 Inch FDA UDI

Category: Emesis bag

The ProCure Bag is a disposable device designed for patients to collect and contain their vomit until it's convenient to dispose of it. It's a single-use, implantable-free option available in various sizes and quantities.

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 95495ccc-f500-465e-a729-3681b84d72ef 36 fields · synced Jul 29, 2026