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Accel®

FDA UDI

Class I (US FDA UDI)

by B Braun Interventional Systems, Inc

Identity

Trade Name
ACCEL® FDA UDI
Generic Name
Vascular catheter introduction needle FDA UDI
Device Name
22GA X 15CM CHIBA NEEDL FDA UDI
Model / Reference
612131 FDA UDI
Description
22GA X 15CM CHIBA NEEDL FDA UDI

Identifiers

Catalog Number
612131 FDA UDI
Primary DI / UDI-DI
04046955237364 FDA UDI
FDA Product Code
DWS FDA UDI
GMDN Term
Vascular catheter introduction needle FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
870.4500 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Vascular catheter introduction needle

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

Similar devices

Also classified as Vascular catheter introduction needle.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 56ec19cd-054f-417f-b8bb-6cfcb81be766 37 fields · synced Jun 1, 2026