1688

FDA UDI

Class II (US FDA UDI)

by Stryker Corp.

Identity

Trade Name: 1688 FDA UDI
Generic Name: Endoscope video camera FDA UDI
Device Name: Inline Camera Head, C-Mount FDA UDI
Model / Reference: 1688710105 FDA UDI
Description: Inline Camera Head, C-Mount FDA UDI

Identifiers

Catalog Number: 1688-710-105 FDA UDI
Primary DI / UDI-DI: 07613327419009 FDA UDI
510(k) Number: K182160 FDA UDI
FDA Product Code: GCJ FDA UDI
GMDN Term: Endoscope video camera 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

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

FDA UDI

Category: Endoscope video camera

1688 by Stryker Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Cleared under the same submission

K182160 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Stryker Corp.

Sources (1)

FDA UDI d40187b8-5aff-4321-b6d1-2994a150fc17 36 fields · synced May 30, 2026