Stimuplex®

Primary DI
04022495166579
Brand
Stimuplex®
Company
B. BRAUN MEDICAL INC.
Model
4894367
Catalog number
4894367
Device description
Stimuplex® A, 30° bevel (4894367)
Published
2016-09-23
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
BXNSTIMULATOR, NERVE, BATTERY-POWERED

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
BXNStimulator, Nerve, Battery-PoweredAnesthesiology2

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
04022495166579PrimaryGS10
04022495166562Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
04022495166579040224951665794022495166579
04022495166562040224951665624022495166562

GMDN Terms#

Term, Definition table
TermDefinition
Peripheral nerve-block blunt needleA sterile slender hand-held metal tube with a dull, straight or bent (coude) tip designed to atraumatically access a peripheral nerve for the injection of an anaesthetic/analgesic agent for nerve-block/pain control (e.g., sleeve blocks, deep muscle blocks, hypogastric blocks, paravertebral blocks, joint blocks, selective nerve root, lumbar sympathetic, Coeliac plexus). It may be used to deliver anaesthetic or analgesic agents directly and/or to allow introduction of a dedicated catheter for administration. This is a single-use device.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Device Size Text, specify0

Storage And Handling#

Type, Low, High table
TypeLowHighCondition
Special Storage Condition, Specify00
Special Storage Condition, Specify00Keep away from sunlight
Special Storage Condition, Specify00Keep dry

Contacts#

Phone, Email table
PhoneEmail
+1(800)227-2862BBMUS_Service.EmailOrders@bbraun.com

Regulatory Flags#

DUNS number
002397347
Device count
25
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
false
Expiration date on label
true
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
04046955966295Design Options®5522105522102026-10-18
04022495101167Stimuplex®489425148942512016-09-23
04022495101266Stimuplex®489427848942782016-09-23
04022495101310Stimuplex®489450248945022016-09-23
04022495187826Stimuplex®489453948945392016-09-23
04046955665075Extension Set4906304906302021-02-08
04046964991257Extension Set4904864904862017-04-03
04046955270347IV Administration Set4905504905502019-02-22
04046955287475IV Administration Set4905744905742018-10-05
04046955203307IV Administration Set4905294905292018-06-15
04046964296734Extension Set4565224565222016-09-23
04046955874330INTROCAN SAFETY®4251610-024251610-022026-10-11
04046955765164IV Administration Set4906404906402026-09-27
04046955114559IV Administration Set4905014905012026-09-19
04046955862658Design Options®5522045522042026-08-17
04046955966233Design Options®5302095302092026-08-17
04046955966370Design Options®5703615703612026-08-17
04046961025153Prontosan®4006044006042026-08-09
04046964176982CONTIPLEX®3317063317062016-09-23
04046964176968CONTIPLEX®3317013317012016-09-23

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06009880396191BIONESSXAVANT TECHNOLOGY (PTY) LTDBXN2025-02-17
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06009880396870STIMPODXAVANT TECHNOLOGY (PTY) LTDBXN2023-12-23
10889483000014SunMedSUNMED, LLCBXN2023-08-01
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