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Reflex

FDA UDI

Class II (US FDA UDI)

by Conmed Corporation

Identity

Trade Name
REFLEX FDA UDI
Generic Name
Laparoscopic access cannula seal reducer, single-use FDA UDI
Device Name
REFLEX 5/12MM UNIVERSAL CONVERTER FDA UDI
Model / Reference
1700 FDA UDI
Description
REFLEX 5/12MM UNIVERSAL CONVERTER FDA UDI

Identifiers

Catalog Number
1700 FDA UDI
Primary DI / UDI-DI
10653405035176 FDA UDI
510(k) Number
K924761 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Laparoscopic access cannula seal reducer, single-use 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

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

Category: Laparoscopic access cannula seal reducer, single-use

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

Similar devices

Also classified as Laparoscopic access cannula seal reducer, single-use.

Cleared under the same submission

K924761 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Conmed Corporation

Sources (1)

  • FDA UDI a30695ab-7473-4316-99d7-e63cef9f6c6a 38 fields · synced Jun 6, 2026