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Halyard

FDA UDI

Class I (US FDA UDI)

by GRI Medical & Electronic Technology Co., Ltd.

Identity

Trade Name
HALYARD FDA UDI
Generic Name
Contaminated waste container FDA UDI
Device Name
Drawcord Bag_Green_40inx40in_2.5mil_N/S_100ea/cs FDA UDI
Model / Reference
68488-80 FDA UDI
Description
Drawcord Bag_Green_40inx40in_2.5mil_N/S_100ea/cs FDA UDI

Identifiers

Primary DI / UDI-DI
16931918142395 FDA UDI
FDA Product Code
FNY FDA UDI
GMDN Term
Contaminated waste container 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Contaminated waste container

Halyard by GRI Medical & Electronic Technology Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Contaminated waste container.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 8971c915-ce28-4a2d-b926-e97319f48378 34 fields · synced Sep 18, 2026