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Trogard Finesse

FDA UDI

Class II (US FDA UDI)

by Conmed Corporation

Identity

Trade Name
TROGARD FINESSE FDA UDI
Generic Name
Laparoscopic access cannula, single-use FDA UDI
Device Name
TROGARD MINI-FINESSE DILATING CONICAL BLUNT TIP LAPAROSCOPIC ACCESS SYSTEM, 5MM FDA UDI
Model / Reference
60-6050-016 FDA UDI
Description
TROGARD MINI-FINESSE DILATING CONICAL BLUNT TIP LAPAROSCOPIC ACCESS SYSTEM, 5MM FDA UDI

Identifiers

Catalog Number
60-6050-016 FDA UDI
Primary DI / UDI-DI
10653405036425 FDA UDI
510(k) Number
K001597 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Laparoscopic access cannula, single-use 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

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Trogard Finesse by Conmed Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Conmed Corporation

Sources (1)

  • FDA UDI 827b2778-3d10-42e2-ad2d-9060fa7b1ac0 39 fields · synced Jun 1, 2026