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Navsuite

FDA UDI

Class II (US FDA UDI)

by Stryker Leibinger

Identity

Trade Name
NAVSUITE FDA UDI
Generic Name
Electrical-only medical device connection cable, reusable FDA UDI
Device Name
NavSuite¿3 Cable for Camera Arm 15FT FDA UDI
Model / Reference
7700-009-101 FDA UDI
Description
NavSuite¿3 Cable for Camera Arm 15FT FDA UDI

Identifiers

Catalog Number
7700-009-101 FDA UDI
Primary DI / UDI-DI
07613327114959 FDA UDI
FDA Product Code
OLO FDA UDI
GMDN Term
Electrical-only medical device connection cable, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4560 FDA UDI
Commercial Distribution
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

Category: Electrical-only medical device connection cable, reusable

Navsuite by Stryker Leibinger — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrical-only medical device connection cable, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stryker Leibinger

Sources (1)

  • FDA UDI f4b0cfcf-7423-4d03-8f57-d0bf2c53e7ce 34 fields · synced May 30, 2026