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Pencan®

FDA UDI

Class II (US FDA UDI)

by B. Braun Medical Inc.

Identity

Trade Name
PENCAN® FDA UDI
Generic Name
Spinal needle, single-use FDA UDI
Device Name
Pencan® 24 Ga. x 4 in (100 mm) Spinal Needle with 20 Ga. Introducer FDA UDI
Model / Reference
333884 FDA UDI
Description
Pencan® 24 Ga. x 4 in (100 mm) Spinal Needle with 20 Ga. Introducer FDA UDI

Identifiers

Catalog Number
333884 FDA UDI
Primary DI / UDI-DI
04046964181047 FDA UDI
FDA Product Code
BSP FDA UDI
GMDN Term
Spinal needle, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5150 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: Spinal needle, single-use

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

Similar devices

Also classified as Spinal needle, single-use.

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 a477d76c-dca9-43d9-93aa-6a802cc684c9 36 fields · synced Jun 8, 2026