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Emesis Bag

FDA UDI

Class I (US FDA UDI)

by Dynarex Corp.

Identity

Trade Name
Emesis Bag FDA UDI
Generic Name
Emesis bag FDA UDI
Device Name
Emesis Bag, White, 1000 cc per bag FDA UDI
Model / Reference
4708 FDA UDI
Description
Emesis Bag, White, 1000 cc per bag FDA UDI

Identifiers

Primary DI / UDI-DI
00616784470832 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

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: Emesis bag

Emesis Bag by Dynarex Corp. — 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
Dynarex Corp.

Sources (1)

  • FDA UDI ae2701a0-1c6c-4fa9-9e63-f3c5add51dce 33 fields · synced May 31, 2026