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Adapt

FDA UDI

Class I (US FDA UDI)

by Stryker Leibinger

Identity

Trade Name
ADAPT FDA UDI
Generic Name
Electrical-only medical device connection cable, reusable FDA UDI
Device Name
Digital Port Connector FDA UDI
Model / Reference
0101-2200 FDA UDI
Description
Digital Port Connector FDA UDI

Identifiers

Catalog Number
0101-2200 FDA UDI
Primary DI / UDI-DI
07613327505245 FDA UDI
FDA Product Code
OUG FDA UDI
GMDN Term
Electrical-only medical device connection cable, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6310 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electrical-only medical device connection cable, reusable

Adapt by Stryker Leibinger — Class I — 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 d3c52698-e389-4512-b4a1-a3e3bf3b70b6 35 fields · synced May 30, 2026