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Ultraplex 360®

FDA UDI

Class II (US FDA UDI)

by B. Braun Medical Inc.

Identity

Trade Name
Ultraplex 360® FDA UDI
Generic Name
Peripheral nerve-block blunt needle FDA UDI
Device Name
22GA X 2 ULTRAPLEX 360 NEEDLE NRFIT FDA UDI
Model / Reference
339205 FDA UDI
Description
22GA X 2 ULTRAPLEX 360 NEEDLE NRFIT FDA UDI

Identifiers

Catalog Number
339205 FDA UDI
Primary DI / UDI-DI
04046955129959 FDA UDI
FDA Product Code
BSP FDA UDI
GMDN Term
Peripheral nerve-block blunt needle FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5150 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: Peripheral nerve-block blunt needle

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

Similar devices

Also classified as Peripheral nerve-block blunt needle.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 669514fc-40b3-4205-8ef8-04cf7de871e1 36 fields · synced Jun 8, 2026