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In'tech Medical SAS

FDA UDI

Class I (US FDA UDI)

by In'tech Medical

Identity

Trade Name
In'tech Medical SAS FDA UDI
Generic Name
Surgical irrigation/aspiration cannula, non-illuminating, reusable FDA UDI
Device Name
Suction Tube #12 FDA UDI
Model / Reference
S06ITM279-C628 FDA UDI
Description
Suction Tube #12 FDA UDI

Identifiers

Primary DI / UDI-DI
03664888000094 FDA UDI
FDA Product Code
GEA FDA UDI
GMDN Term
Surgical irrigation/aspiration cannula, non-illuminating, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical irrigation/aspiration cannula, non-illuminating, reusable

In'tech Medical SAS by In'tech Medical — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical irrigation/aspiration cannula, non-illuminating, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
In'tech Medical

Sources (1)

  • FDA UDI 6dac9851-f52b-4703-936b-fe737b55f762 34 fields · synced May 30, 2026