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Alleset

FDA UDI

Class II (US FDA UDI)

by GRI Medical & Electronic Technology Co., Ltd.

Identity

Trade Name
Alleset FDA UDI
Generic Name
Instrument management bag FDA UDI
Device Name
Diathermy Pouch_50x60cm_1-Pocket_w/ Adhesive_250ea/cs FDA UDI
Model / Reference
Model 80-14815 FDA UDI
Description
Diathermy Pouch_50x60cm_1-Pocket_w/ Adhesive_250ea/cs FDA UDI

Identifiers

Primary DI / UDI-DI
16931918177731 FDA UDI
FDA Product Code
PUI FDA UDI
GMDN Term
Instrument management bag FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4370 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: Instrument management bag

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 Instrument management bag.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3772464e-2840-4e46-8b19-7edca51d3106 34 fields · synced Sep 18, 2026