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Accel®

FDA UDI

Class II (US FDA UDI)

by B Braun Interventional Systems, Inc

Identity

Trade Name
ACCEL® FDA UDI
Generic Name
Multi-purpose percutaneous abdominothoracic drainage catheter FDA UDI
Device Name
ACCEL APD 8F 25CM W/ LOCK FDA UDI
Model / Reference
613902 FDA UDI
Description
ACCEL APD 8F 25CM W/ LOCK FDA UDI

Identifiers

Catalog Number
613902 FDA UDI
Primary DI / UDI-DI
04046955638390 FDA UDI
FDA Product Code
FGE FDA UDI
GBO FDA UDI
GMDN Term
Multi-purpose percutaneous abdominothoracic drainage catheter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5010 FDA UDI
878.4200 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Multi-purpose percutaneous abdominothoracic drainage catheter

Accel® by B Braun Interventional Systems, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multi-purpose percutaneous abdominothoracic drainage catheter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
B Braun Interventional Systems, Inc

Sources (1)

  • FDA UDI ed495c6b-1b1f-4fb8-93bb-fe52de67945e 36 fields · synced May 30, 2026