STERiJECT TM

Primary DI
14571225316199
Brand
STERiJECT TM
Company
TSK LABORATORY, JAPAN
Model
PRC-30013IN
Device description
TSK STERiJECT Premium Disposable Hypodermic Needle
Published
2017-12-20
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
false
OTC
true
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

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K970370000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K970370000TSK STERIJEKT PREMIUM DISPOSABLE HYPODERMIC NEEDLETsk Laboratory, Japan1997-04-10FMI

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
14571225316199PackageGS160In Commercial Distribution
04571225316192PrimaryGS10
04571225316185Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
1457122531619914571225316199
04571225316192045712253161924571225316192
04571225316185045712253161854571225316185

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
Outer Diameter0.3Millimeter

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
716217877
Device count
100
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
true
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
04580708068527STERiJECT TMPRE-25013I2026-01-15
04580708068534STERiJECT TMPRE-25013I2026-01-15
14580708068524STERiJECT TMPRE-25013I2026-01-15
24580708068538STERiJECT TMPRE-25013I2026-01-15
04580708067445STERiJECT TMLDS-27006I2025-08-18
14580708067442STERiJECT TMLDS-27006I2025-08-18
04571225317625STERiJECT TMHPC-31013E2024-06-11
14571225317622STERiJECT TMHPC-31013E2024-06-11
14571225314157STERiJECT TMHPC-27013I2024-06-10
14571225314218STERiJECT TMHPC-30013I2024-06-10
04571225314105STERiJECT TMHPC-23013I2024-06-10
04571225314112STERiJECT TMHPC-23013I2024-06-10
04571225314198STERiJECT TMHPC-27019I2024-06-10
04571225314204STERiJECT TMHPC-27019I2024-06-10
04571225314235STERiJECT TMHPC-30013I2024-06-10
04571225317779STERiJECT TMHPC-23013I2024-06-10
04571225317793STERiJECT TMHPC-27013I2024-06-10
04571225317809STERiJECT TMHPC-27019I2024-06-10
04571225317816STERiJECT TMHPC-29010E2024-06-10
04571225317823STERiJECT TMHPC-29013E2024-06-10

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