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Contiplex® Ultra 360®

FDA UDI

Class II (US FDA UDI)

by B. Braun Medical Inc.

Identity

Trade Name
Contiplex® Ultra 360® FDA UDI
Generic Name
Peripheral anaesthesia catheter set, medicated FDA UDI
Device Name
18G x 4 CONT UTRA 360 20G EC CATH NRFIT FDA UDI
Model / Reference
339220 FDA UDI
Description
18G x 4 CONT UTRA 360 20G EC CATH NRFIT FDA UDI

Identifiers

Catalog Number
339220 FDA UDI
Primary DI / UDI-DI
04046955130252 FDA UDI
FDA Product Code
OGJ FDA UDI
GMDN Term
Peripheral anaesthesia catheter set, medicated 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

Yes

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
MRI Safety
MR Unsafe FDA UDI

Category: Peripheral anaesthesia catheter set, medicated

Contiplex® Ultra 360® by B. Braun Medical Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Peripheral anaesthesia catheter 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 8b7cfcbf-07ac-437a-ba56-9ce76ad8411a 37 fields · synced May 31, 2026