Quicklatch

FDA UDIEUDAMED

Class II (US FDA UDI)

by Conmed Corporation

Identity

Trade Name: QUICKLATCH FDA UDI
Generic Name: Rigid optical arthroscope, reusable FDA UDI
Device Name: QUICKLATCH AUTOCLAVABLE EYECUP SCOPE, 4 MM, 30° FDA UDI
Model / Reference: QL4300 FDA UDI
Description: QUICKLATCH AUTOCLAVABLE EYECUP SCOPE, 4 MM, 30° FDA UDI

Identifiers

Catalog Number: QL4300 FDA UDI
Primary DI / UDI-DI: 10845854013137 FDA UDI
510(k) Number: K962075 FDA UDI
FDA Product Code: HRX FDA UDI
GMDN Term: Rigid optical arthroscope, reusable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.1100 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size: Angle — 30 degree FDA UDI
Outer Diameter — 4 Millimeter FDA UDI

Category: Rigid optical arthroscope, reusable

Quicklatch by Conmed Corporation — Class II — MDD, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Rigid optical arthroscope, reusable.

Arthrex® — Arthrex, Inc. · Class II
AED — NATIONAL ADVANCED ENDOSCOPY DEVICES, INC. · Class II
Arthrex® — Arthrex, Inc. · Class II
HOPKINS — Karl Storz GmbH & Co. KG · Class II
Olympus — Olympus Winter & Ibe GmbH · Class II
Surgical Direct — SURGICAL DIRECT, INC. · Class II
HOPKINS — Karl Storz GmbH & Co. KG · Class II
Precision Ideal Eyes — Stryker Corp. · Class II

Cleared under the same submission

K962075 also covers:

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDD

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
EUDAMED	European Union	MDD	—	Class II	Unknown
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Conmed Corporation

Sources (2)

FDA UDI 6846ad31-1fec-40a3-9f32-3af657905ad9 37 fields · synced May 31, 2026
EUDAMED 1 fields · synced May 29, 2026