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Stimuplex®

FDA UDI

Class II (US FDA UDI)

by B. Braun Medical Inc.

Identity

Trade Name
Stimuplex® FDA UDI
Generic Name
Nerve-locating anaesthesia needle FDA UDI
Device Name
Stimuplex® Ultra 22 Ga. x4 in. (100 mm) Insulated Echogenic Needle with 30° Bevel and Extension Set (STIMAU22100/30) FDA UDI
Model / Reference
333656 FDA UDI
Description
Stimuplex® Ultra 22 Ga. x4 in. (100 mm) Insulated Echogenic Needle with 30° Bevel and Extension Set (STIMAU22100/30) FDA UDI

Identifiers

Catalog Number
333656 FDA UDI
Primary DI / UDI-DI
04046964180187 FDA UDI
FDA Product Code
BSP FDA UDI
GMDN Term
Nerve-locating anaesthesia 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: Nerve-locating anaesthesia needle

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

Similar devices

Also classified as Nerve-locating anaesthesia needle.

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 8325fd5b-cbf8-42e8-b64c-57a23d9d4a0e 36 fields · synced May 30, 2026