Spinocan®

Primary DI
04046955768219
Brand
Spinocan®
Company
B. BRAUN MEDICAL INC.
Model
339235
Catalog number
339235
Device description
22GA X 6 SPINAL NEEDLE NRFIT
Published
2023-06-23
Public version status
New
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
BSPNEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER)

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
BSPNeedle, Conduction, Anesthetic (W/Wo Introducer)Anesthesiology2

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
04046955768226PrimaryGS10
04046955768219Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
04046955768226040469557682264046955768226
04046955768219040469557682194046955768219

GMDN Terms#

Term, Definition table
TermDefinition
Spinal needle, single-useA sterile, sharp bevel-edged, hollow tubular metal instrument designed to deliver anaesthetic or analgesic agents intrathecally (in the space under the arachnoid membrane of the brain and spinal cord), withdraw a sample of cerebrospinal fluid (CSF), and/or assist introduction of an intrathecal catheter (e.g., lumboperitoneal shunt, spinal catheter). It is typically fenestrated, spring-tipped, and used for short-term administration; it is typically made of metal and plastic materials. This is a single-use device.

Device Sizes#

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

Sterilization Methods#

Method table
Method

Contacts#

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

Regulatory Flags#

DUNS number
002397347
Device count
50
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
true
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
04046964813993Design Options®5301605301602016-09-23
04022495101211Stimuplex®489426048942602016-09-23
04046955966295Design Options®5522105522102026-10-18
04022495101167Stimuplex®489425148942512016-09-23
04022495101266Stimuplex®489427848942782016-09-23
04022495101310Stimuplex®489450248945022016-09-23
04022495166579Stimuplex®489436748943672016-09-23
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

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