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Connexion

FDA UDI

Class II (US FDA UDI)

by 3C-Medical Intelligence GmbH

Identity

Trade Name
Connexion FDA UDI
Generic Name
Accelerator system table, non-powered FDA UDI
Device Name
The Short Indexing bar is required for accurate repositioning of accessories at the middle area of the Connexion™ Lateral Opening Module. FDA UDI
Model / Reference
P10105-253 FDA UDI
Description
The Short Indexing bar is required for accurate repositioning of accessories at the middle area of the Connexion™ Lateral Opening Module. FDA UDI

Identifiers

Catalog Number
P10105-253 FDA UDI
Primary DI / UDI-DI
04056719001261 FDA UDI
FDA Product Code
IXQ FDA UDI
GMDN Term
Accelerator system table, non-powered FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1980 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

Yes

FDA UDI

Category: Accelerator system table, non-powered

Connexion by 3C-Medical Intelligence GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Accelerator system table, non-powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
3C-Medical Intelligence GmbH

Sources (1)

  • FDA UDI 4ddbd505-b8da-4ffc-9456-d892998a5203 34 fields · synced Jun 8, 2026