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Diversatek Healthcare

FDA UDI

Class II (US FDA UDI)

by Diversatek Healthcare

Identity

Trade Name
Diversatek Healthcare FDA UDI
Generic Name
Suction/irrigation tubing, single-use FDA UDI
Device Name
1/4" ID x 100 FT Universal Funnel Tubing, Non-Conductive FDA UDI
Model / Reference
1268-02 FDA UDI
Description
1/4" ID x 100 FT Universal Funnel Tubing, Non-Conductive FDA UDI

Identifiers

Catalog Number
1268-02 FDA UDI
Primary DI / UDI-DI
M7831268021 FDA UDI
FDA Product Code
GAZ FDA UDI
GMDN Term
Suction/irrigation tubing, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Lumen/Inner Diameter — 0.25 Inch FDA UDI

Category: Suction/irrigation tubing, single-use

Diversatek Healthcare by Diversatek Healthcare — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Suction/irrigation tubing, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 24eeec8f-c56d-4eb1-80dc-d6955f2d0d15 36 fields · synced Jun 1, 2026