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Alleset

FDA UDI

Class I (US FDA UDI)

by GRI Medical & Electronic Technology Co., Ltd.

Identity

Trade Name
Alleset FDA UDI
Generic Name
General-purpose bowl, single-use FDA UDI
Device Name
Sustainable Medicine Cup_150cc_Non-sterile1000ea/cs FDA UDI
Model / Reference
Ei15-0150 FDA UDI
Description
Sustainable Medicine Cup_150cc_Non-sterile1000ea/cs FDA UDI

Identifiers

Primary DI / UDI-DI
16931918182759 FDA UDI
FDA Product Code
KYW FDA UDI
GMDN Term
General-purpose bowl, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6430 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: General-purpose bowl, single-use

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

Similar devices

Also classified as General-purpose bowl, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
GRI Medical & Electronic Technology Co., Ltd.

Sources (1)

  • FDA UDI 185099b8-6745-48b7-9a12-1e43a840488a 34 fields · synced Sep 18, 2026