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Mictec Injection Cannula

FDA UDI

Class II (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
MICTEC INJECTION CANNULA FDA UDI
Generic Name
Laparoscopic access cannula, reusable FDA UDI
Device Name
MICTEC INJECTION CANNULA CURVED SMALL LUER LOCK G22 FDA UDI
Model / Reference
20941-01 FDA UDI
Description
MICTEC INJECTION CANNULA CURVED SMALL LUER LOCK G22 FDA UDI

Identifiers

Primary DI / UDI-DI
00192896008731 FDA UDI
510(k) Number
K002877 FDA UDI
FDA Product Code
HET FDA UDI
GMDN Term
Laparoscopic access cannula, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.1720 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

No

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 — 300 Millimeter FDA UDI

Category: Laparoscopic access cannula, reusable

Mictec Injection Cannula by Sontec Instruments, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Laparoscopic access cannula, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c58ddd5a-99d7-421a-8d25-5c02e0fd44a5 36 fields · synced Jun 8, 2026