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Sterican™

FDA UDI

Class I (US FDA UDI)

by B. Braun Medical Inc.

Identity

Trade Name
STERICAN™ FDA UDI
Generic Name
Medication transfer needle, non-filtering/non-vented FDA UDI
Device Name
STERICAN 18G,1.20X40MM BLUNT-US FDA UDI
Model / Reference
4038088-02 FDA UDI
Description
STERICAN 18G,1.20X40MM BLUNT-US FDA UDI

Identifiers

Catalog Number
4038088-02 FDA UDI
Primary DI / UDI-DI
04046964041198 FDA UDI
FDA Product Code
GAA FDA UDI
GMDN Term
Medication transfer needle, non-filtering/non-vented FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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: Medication transfer needle, non-filtering/non-vented

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

Similar devices

Also classified as Medication transfer needle, non-filtering/non-vented.

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 189d7b48-ecc2-4a87-8a96-0e7fdc24bedc 36 fields · synced May 30, 2026