Alleset

FDA UDI

Class I (US FDA UDI)

by GRI Medical & Electronic Technology Co., Ltd.

Identity

Trade Name: Alleset FDA UDI
Generic Name: Insufflation gas conditioning tubing set FDA UDI
Device Name: Insufflation Tubing 12ft(3.7m) with 0.1-micron Hi-Flow Filter_Rotating Luer Lock Fitting_NS_100ea/cs FDA UDI
Model / Reference: Model C-2012-NS FDA UDI
Description: Insufflation Tubing 12ft(3.7m) with 0.1-micron Hi-Flow Filter_Rotating Luer Lock Fitting_NS_100ea/cs FDA UDI

Identifiers

Primary DI / UDI-DI: 16931918141152 FDA UDI
FDA Product Code: NKC FDA UDI
GMDN Term: Insufflation gas conditioning tubing set FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 884.1730 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Insufflation gas conditioning tubing set

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

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: GRI Medical & Electronic Technology Co., Ltd.

Sources (1)

FDA UDI 022915ed-1ee3-4df9-88c4-678015ce3a77 34 fields · synced Sep 18, 2026