FDA.reportPublic FDA data

HSW HENKE-JECT®

Primary DI
04035873059066
Brand
HSW HENKE-JECT®
Company
Henke-Sass, Wolf GmbH
Model
4710008040
Catalog number
4710008040
Device description
HSW HENKE-JECT® 21G X 1 1/2 - 0,80 X 40 MM
Published
2020-12-09
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

Product Codes#

Code, Name table
CodeName
FMINeedle, Hypodermic, Single Lumen

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
FMINeedle, Hypodermic, Single LumenGeneral Hospital2

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
04035873059066PackageGS130In Commercial Distribution
04035873059059PrimaryGS10
04035873059042Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
04035873059066040358730590664035873059066
04035873059059040358730590594035873059059
04035873059042040358730590424035873059042

GMDN Terms#

Term, Definition table
TermDefinition
Hypodermic needle, single-useA non-dedicated, sharp bevel-edged, hollow tubular device intended to be inserted beneath the skin of a patient while connected to a noninvasive device (e.g., syringe, secondary medication set) to administer and/or withdraw (aspirate) fluids/drugs; it may also be used for fluid/drug preparation. Some types are designed with a shielding mechanism (e.g., safety cap) for protection from sharp injuries. It is not specifically designed for blood collection or artery puncture, and does not have wings for fixation/placement (i.e., not a blood collection, intra-arterial, or venous butterfly needle). This is a single-use device.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Length40Millimeter
Outer Diameter0.8Millimeter

Storage And Handling#

Type, Low, High table
TypeLowHighCondition
Special Storage Condition, Specify00PROTECT FROM SUNLIGHT, KEEP DRY

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
317326411
Device count
100
DM exempt
true
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
04035873059776HSW HENKE-JECT®485000300048500030002020-12-09
04035873055549NA830003857183000385712017-08-04
04035873055556NA830003857283000385722017-08-04
04035873055563NA830003857383000385732017-08-04
04035873055570NA830003857483000385742017-08-04
04035873055587NA830003857583000385752017-08-04
04035873055594NA830003857683000385762017-08-04
04035873055600NA830003857883000385782017-08-04
04035873055617NA830003874583000387452017-08-04
04035873068709N/A830005352083000535202021-02-19
04035873068723N/A830005352283000535222021-02-19
04035873068730N/A830005352383000535232021-02-19
04035873069188N/A830005490883000549082021-02-19
04035873068679N/A830005351783000535172021-02-18
04035873068686N/A830005351883000535182021-02-18
04035873068693N/A830005351983000535192021-02-18
04035873068716N/A830005352183000535212021-02-18
04035873067788N/A830005474983000547492021-02-16
04035873066538N/A830005347583000534752021-02-12
04035873066569N/A830005347883000534782021-02-12

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