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Adapt

FDA UDI

Class II (US FDA UDI)

by Stryker Leibinger

Identity

Trade Name
ADAPT FDA UDI
Generic Name
Medical image management system FDA UDI
Device Name
PC Unit FDA UDI
Model / Reference
0101-2900 FDA UDI
Description
PC Unit FDA UDI

Identifiers

Catalog Number
0101-2900 FDA UDI
Primary DI / UDI-DI
07613327312393 FDA UDI
FDA Product Code
HSB FDA UDI
OLO FDA UDI
GMDN Term
Medical image management system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3020 FDA UDI
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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Medical image management system

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

Similar devices

Also classified as Medical image management system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stryker Leibinger

Sources (1)

  • FDA UDI 3fab4b2b-fcb0-47f3-82a3-a9561649a568 34 fields · synced Jun 6, 2026