← Back to catalogue

Inflow Cannula Set

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
INFLOW CANNULA SET FDA UDI
Generic Name
Arthroscopic access cannula, reusable FDA UDI
Device Name
INFLOW CANNULA SET WITH ADAPTOR FDA UDI
Model / Reference
SC95-0302-SET FDA UDI
Description
INFLOW CANNULA SET WITH ADAPTOR FDA UDI

Identifiers

Catalog Number
SC95-0302-SET FDA UDI
Primary DI / UDI-DI
00192896094864 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Arthroscopic access cannula, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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

No

FDA UDI

Dimensions & Sizes

Size
Length — 5.5 Inch FDA UDI

Category: Arthroscopic access cannula, reusable

Inflow Cannula Set by Sontec Instruments, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Arthroscopic access cannula, reusable.

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

Manufacturer
Sontec Instruments, Inc.

Sources (1)

  • FDA UDI 33b4195f-c639-4b4f-a1d8-555b21d492d9 36 fields · synced Jun 6, 2026