Accel®

FDA UDI

Class I (US FDA UDI)

by B. Braun Medical Inc.

Identity

Trade Name: ACCEL® FDA UDI
Generic Name: Peritoneal drainage catheter FDA UDI
Device Name: ACCEL VALVED CENTESIS 5FX15CM 20G FDA UDI
Model / Reference: 613154 FDA UDI
Description: ACCEL VALVED CENTESIS 5FX15CM 20G FDA UDI

Identifiers

Catalog Number: 613154 FDA UDI
Primary DI / UDI-DI: 04046955621804 FDA UDI
FDA Product Code: GCB FDA UDI
GMDN Term: Peritoneal drainage catheter FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4200 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Peritoneal drainage catheter

Accel® by B. Braun Medical Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Peritoneal drainage catheter.

ASEPT Peritoneal Drainage System — PFM MEDICAL INCORPORATED · Class I
Grafco — GF Health Products, Inc · Class I
TAUT — TELEFLEX INCORPORATED · Class I
TAUT — TELEFLEX INCORPORATED · Class I
ACCEL™ — B BRAUN INTERVENTIONAL SYSTEMS, INC · Class I
TAUT — TELEFLEX INCORPORATED · Class I
TAUT — TELEFLEX INCORPORATED · Class I
ACCEL™ — B BRAUN INTERVENTIONAL SYSTEMS, INC · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: B. Braun Medical Inc.

Sources (1)

FDA UDI 6ea33a18-b6dd-4df9-b2db-785e7790432e 35 fields · synced Jun 1, 2026