← Back to catalogue

Perifix®

FDA UDI

Class I (US FDA UDI)

by B. Braun Medical Inc.

Identity

Trade Name
Perifix® FDA UDI
Generic Name
Wearable percutaneous catheter/tube holder FDA UDI
Device Name
PERIFIX® PinPad™ - securement device for PERIFIX 0.2 µm Flat Epidural Filter FDA UDI
Model / Reference
415004 FDA UDI
Description
PERIFIX® PinPad™ - securement device for PERIFIX 0.2 µm Flat Epidural Filter FDA UDI

Identifiers

Catalog Number
415004 FDA UDI
Primary DI / UDI-DI
04046964183232 FDA UDI
FDA Product Code
KMK FDA UDI
GMDN Term
Wearable percutaneous catheter/tube holder FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5210 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

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: Wearable percutaneous catheter/tube holder

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

Similar devices

Also classified as Wearable percutaneous catheter/tube holder.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 2544f099-66e5-45b6-8546-86ed12c40c35 35 fields · synced May 29, 2026