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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
Epidural anaesthesia set, medicated FDA UDI
Device Name
PERIFIX® 18 Ga. x 3-1/2 in. (90 mm) Hustead, 5 mL Glass Luer Lock LOR Tray (Kit) FDA UDI
Model / Reference
332249 FDA UDI
Description
PERIFIX® 18 Ga. x 3-1/2 in. (90 mm) Hustead, 5 mL Glass Luer Lock LOR Tray (Kit) FDA UDI

Identifiers

Catalog Number
332249 FDA UDI
Primary DI / UDI-DI
04046964178702 FDA UDI
FDA Product Code
OGE FDA UDI
GMDN Term
Epidural anaesthesia set, 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: Epidural anaesthesia set, medicated

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

Similar devices

Also classified as Epidural anaesthesia set, medicated.

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 1a8211e8-9c0d-4feb-b41a-024ba4f6614a 37 fields · synced May 31, 2026