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Flexible Trocar Sleeve

FDA UDI

Class II (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
FLEXIBLE TROCAR SLEEVE FDA UDI
Generic Name
Laparoscopic multi-instrument access port, reusable FDA UDI
Device Name
FLEXIBLE TROCAR SLEEVE FDA UDI
Model / Reference
15-16141-06 FDA UDI
Description
FLEXIBLE TROCAR SLEEVE FDA UDI

Identifiers

Primary DI / UDI-DI
B0991516141065 FDA UDI
510(k) Number
K002877 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Laparoscopic multi-instrument access port, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 FDA UDI
Commercial Distribution
Not 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 — 100 Millimeter FDA UDI
Width — 10.5 Millimeter FDA UDI

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

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 c277fbbc-b12d-4d71-b1e3-a925fb554516 37 fields · synced May 31, 2026