Stimuplex® Ultra 360®

FDA UDI

Class II (US FDA UDI)

by B. Braun Medical Inc.

Identity

Trade Name: Stimuplex® Ultra 360® FDA UDI
Generic Name: Peripheral nerve-block blunt needle FDA UDI
Device Name: Stimuplex® Ultra 360® 22 Ga. x 1-3/8 in. (35 mm) Insulated Echogenic Needle with 30° Beveland and Extension Set (STIMU32235) FDA UDI
Model / Reference: 333640 FDA UDI
Description: Stimuplex® Ultra 360® 22 Ga. x 1-3/8 in. (35 mm) Insulated Echogenic Needle with 30° Beveland and Extension Set (STIMU32235) FDA UDI

Identifiers

Catalog Number: 333640 FDA UDI
Primary DI / UDI-DI: 04046964726538 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

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Peripheral nerve-block blunt needle

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

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: B. Braun Medical Inc.

Sources (1)

FDA UDI f8d5c680-45cd-4cb5-89a6-93bfb07ccf59 35 fields · synced May 31, 2026