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Mictec Oval Trocar

FDA UDI

Class II (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
MICTEC OVAL TROCAR FDA UDI
Generic Name
Laparoscopic trocar blade, reusable FDA UDI
Device Name
MICTEC OVAL TROCAR FOR ENDO STAPLER WAVED FDA UDI
Model / Reference
20913-18 FDA UDI
Description
MICTEC OVAL TROCAR FOR ENDO STAPLER WAVED FDA UDI

Identifiers

Catalog Number
20913-18 FDA UDI
Primary DI / UDI-DI
00192896007888 FDA UDI
510(k) Number
K002877 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Laparoscopic trocar blade, 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 — 13 Millimeter FDA UDI
Length — 70 Millimeter FDA UDI

Category: Laparoscopic trocar blade, reusable

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

Similar devices

Also classified as Laparoscopic trocar blade, 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 a6f59c00-8c01-43d8-873b-555b380b01d5 37 fields · synced May 30, 2026