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Perifix™

FDA UDI

Class II (US FDA UDI)

by B. Braun Medical Inc.

Identity

Trade Name
PERIFIX™ FDA UDI
Generic Name
Neuraxial syringe FDA UDI
Device Name
PERIFIX 10 ML GLASS LOR SYR SLIP NRFIT FDA UDI
Model / Reference
339172 FDA UDI
Description
PERIFIX 10 ML GLASS LOR SYR SLIP NRFIT FDA UDI

Identifiers

Catalog Number
339172 FDA UDI
Primary DI / UDI-DI
04046955735464 FDA UDI
FDA Product Code
CAZ FDA UDI
GMDN Term
Neuraxial syringe 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: Neuraxial syringe

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

Similar devices

Also classified as Neuraxial syringe.

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 68aaa486-cb8d-4463-ba52-e534bb37dc7f 35 fields · synced Jun 8, 2026