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TAP Tubing Set

FDA UDI

Class II (US FDA UDI)

by Northgate Technologies Inc.

Identity

Trade Name
TAP Tubing Set FDA UDI
Generic Name
Endoscopic insufflation tubing set, single-use FDA UDI
Device Name
True Abdominal Pressure Tubing Set for use with Laparoscopic Insufflators with TAP feature. FDA UDI
Model / Reference
7-510-31 FDA UDI
Description
True Abdominal Pressure Tubing Set for use with Laparoscopic Insufflators with TAP feature. FDA UDI

Identifiers

Primary DI / UDI-DI
00817183020356 FDA UDI
510(k) Number
K983326 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

No

FDA UDI

Contains Latex

Yes

FDA UDI

Prescription Use

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Endoscopic insufflation tubing set, single-use

TAP Tubing Set by Northgate Technologies Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscopic insufflation tubing set, single-use.

Cleared under the same submission

K983326 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d6603b0e-1281-470b-94ca-04badbf8e021 34 fields · synced May 30, 2026