Stimuplex®

FDA UDI

Class II (US FDA UDI)

by B. Braun Medical Inc.

Identity

Trade Name: Stimuplex® FDA UDI
Generic Name: Peripheral nerve-block blunt needle FDA UDI
Device Name: Stimuplex® A, 30° bevel (4894260) FDA UDI
Model / Reference: 4894260 FDA UDI
Description: Stimuplex® A, 30° bevel (4894260) FDA UDI

Identifiers

Catalog Number: 4894260 FDA UDI
Primary DI / UDI-DI: 04022495101211 FDA UDI
FDA Product Code: BXN FDA UDI
GMDN Term: Peripheral nerve-block blunt needle FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 868.2775 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® by B. Braun Medical Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Peripheral nerve-block blunt needle.

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Halyard — Avanos Medical, Inc. · Class II
Chiba-Type Spinal Needle — HAKKO CO., LTD. · Class II
Chiba-Type Spinal Needle — HAKKO CO., LTD. · Class II
Chiba-Type Spinal Needle — HAKKO CO., LTD. · Class II
Curved Tip Needle — HAKKO CO., LTD. · Class II

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 53e81b9d-b9b5-43e2-ab2b-fb8edef355f7 36 fields · synced May 30, 2026