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Safecan™

FDA UDI

Class II (US FDA UDI)

by B. Braun Medical Inc.

Identity

Trade Name
SAFECAN™ FDA UDI
Generic Name
Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, drainage FDA UDI
Device Name
Safecan™ Safety Introducer Needle 21G x 2.75 inch, Echogenic Tip, A-Bevel, Sterile FDA UDI
Model / Reference
613107 FDA UDI
Description
Safecan™ Safety Introducer Needle 21G x 2.75 inch, Echogenic Tip, A-Bevel, Sterile FDA UDI

Identifiers

Catalog Number
613107 FDA UDI
Primary DI / UDI-DI
04046964309106 FDA UDI
FDA Product Code
DYB FDA UDI
GMDN Term
Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, drainage FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1340 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

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: Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, drainage

Safecan™ by B. Braun Medical Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, drainage.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
B. Braun Medical Inc.

Sources (1)

  • FDA UDI af4b60df-d694-43c6-951a-1294e1048005 36 fields · synced May 30, 2026