← Back to catalogue

Alleset

FDA UDI

Class II (US FDA UDI)

by GRI Medical & Electronic Technology Co., Ltd.

Identity

Trade Name
Alleset FDA UDI
Generic Name
Isolation gown, single-use FDA UDI
Device Name
AMMI3 Isolation gown_X-Large_40g SMS_Non-sterile_100ea/cs FDA UDI
Model / Reference
60-3073 FDA UDI
Description
AMMI3 Isolation gown_X-Large_40g SMS_Non-sterile_100ea/cs FDA UDI

Identifiers

Primary DI / UDI-DI
16931918188652 FDA UDI
FDA Product Code
FYC FDA UDI
GMDN Term
Isolation gown, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4040 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Isolation gown, single-use

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

Similar devices

Also classified as Isolation gown, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI ec2193f5-aa79-42d2-a5c7-f1c2590efceb 34 fields · synced Sep 18, 2026