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Titanium Mictec Flexible Trocar Set

FDA UDI

Class II (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
TITANIUM MICTEC FLEXIBLE TROCAR SET FDA UDI
Generic Name
Laparoscopic access cannula, reusable FDA UDI
Device Name
TITANIUM MICTEC FLEXIBLE TROCAR SET FDA UDI
Model / Reference
20910-17 FDA UDI
Description
TITANIUM MICTEC FLEXIBLE TROCAR SET FDA UDI

Identifiers

Catalog Number
20910-17 FDA UDI
Primary DI / UDI-DI
00192896007840 FDA UDI
510(k) Number
K002877 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Laparoscopic access cannula, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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
Outer Diameter — 10.5 Millimeter FDA UDI
Length — 70 Millimeter FDA UDI

Category: Laparoscopic access cannula, reusable

Titanium Mictec Flexible Trocar Set 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 c35f8807-602a-49ea-a628-8d921782f6fd 37 fields · synced Jun 1, 2026