Tap

FDA UDI

Class II (US FDA UDI)

by Northgate Technologies Inc.

Identity

Trade Name: TAP FDA UDI
Generic Name: Endoscopic insufflation tubing set, single-use FDA UDI
Device Name: Insufflation Tubing, True Abdominal Pressure Sensing FDA UDI
Model / Reference: 7205836 FDA UDI
Description: Insufflation Tubing, True Abdominal Pressure Sensing FDA UDI

Identifiers

Catalog Number: 72-00153-0 FDA UDI
Primary DI / UDI-DI: 00817183020608 FDA UDI
FDA Product Code: HIF FDA UDI
GMDN Term: Endoscopic insufflation tubing set, single-use FDA UDI

Classification

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

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Endoscopic insufflation tubing set, single-use

Tap by Northgate Technologies Inc. — Class II — 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 II	Pending data

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Manufacturer

Manufacturer: Northgate Technologies Inc.

Sources (1)

FDA UDI 85c6dfbf-8179-4e0e-880d-fe65e982697d 34 fields · synced May 30, 2026