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Epican™

FDA UDI

Class II (US FDA UDI)

by B. Braun Medical Inc.

Identity

Trade Name
EPICAN™ FDA UDI
Generic Name
Epidural needle, non-threaded FDA UDI
Device Name
EPICAN™ 22 Ga. x 1-3/4 in. (35 mm) Caudal Needle - Non-Winged and Clear Hub FDA UDI
Model / Reference
332177 FDA UDI
Description
EPICAN™ 22 Ga. x 1-3/4 in. (35 mm) Caudal Needle - Non-Winged and Clear Hub FDA UDI

Identifiers

Catalog Number
332177 FDA UDI
Primary DI / UDI-DI
04046964177927 FDA UDI
FDA Product Code
CAZ FDA UDI
GMDN Term
Epidural needle, non-threaded FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5140 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: Epidural needle, non-threaded

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

Similar devices

Also classified as Epidural needle, non-threaded.

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 0365e69a-bf31-48a6-8b5a-83f4e6339cf3 36 fields · synced May 30, 2026