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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
Intrathecal anaesthesia set, non-medicated FDA UDI
Device Name
Pencan® 24 Ga. x 4 in. (100 mm), Bupivacaine 0.75% with Dextrose 8.25% Tray (Kit) FDA UDI
Model / Reference
333868 FDA UDI
Description
Pencan® 24 Ga. x 4 in. (100 mm), Bupivacaine 0.75% with Dextrose 8.25% Tray (Kit) FDA UDI

Identifiers

Catalog Number
333868 FDA UDI
Primary DI / UDI-DI
04046964180866 FDA UDI
FDA Product Code
OFU FDA UDI
GMDN Term
Intrathecal anaesthesia set, non-medicated FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5120 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

Yes

FDA UDI

Combination Product

Yes

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: Intrathecal anaesthesia set, non-medicated

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

Similar devices

Also classified as Intrathecal anaesthesia set, non-medicated.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1f26e5b6-f28d-40a6-8ea8-7979baafd629 37 fields · synced Jun 8, 2026