← Back to catalogue

Flo-Assist II

FDA UDI

Class II (US FDA UDI)

by Northgate Technologies Inc.

Identity

Trade Name
Flo-Assist II FDA UDI
Generic Name
Surgical irrigation tubing set, single-use FDA UDI
Device Name
Irrigation Tubing Set FDA UDI
Model / Reference
7-510-49 FDA UDI
Description
Irrigation Tubing Set FDA UDI

Identifiers

Primary DI / UDI-DI
00817183020363 FDA UDI
FDA Product Code
LJH FDA UDI
GMDN Term
Surgical irrigation tubing set, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5130 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: Surgical irrigation tubing set, single-use

Flo-Assist II by Northgate Technologies Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical irrigation tubing set, 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 36c3802f-0761-448c-9143-eac44f1ac1cd 33 fields · synced May 31, 2026