TKMD

Primary DI
06934841565166
Brand
TKMD
Company
Anhui Tiankang Medical Technology Co., Ltd.
Model
TKSLS
Device description
The piston syringe is a device intended for medical purposes, consisting of a calibrated hollow barrel and a movable plunger. At one end of the barrel there is a male Luer Slip /lock connector (nozzle) for attaching the female Luer connector (hub) of a hypodermic single lumen needle, or for attaching other devices with a female Luer. The syringe is sterilized by EtO gas and is labeled Non-Pyrogenic. The device is intended for single use only.
Published
2021-05-28
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
Sterile
true
Single use
true

Product Codes#

Code, Name table
CodeName
FMFSyringe, Piston

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
FMFSyringe, PistonGeneral Hospital2

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
16934841565163PackageGS1100In Commercial Distribution
66934841565168PackageGS118In Commercial Distribution
06934841565166PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
1693484156516316934841565163
6693484156516866934841565168
06934841565166069348415651666934841565166

GMDN Terms#

Term, Definition table
TermDefinition
General-purpose syringe, single-useA sterile device consisting of a calibrated barrel (cylinder) with plunger intended to be used for injection/withdrawal of fluids/gas (e.g., medication) to/from a medical device or the body (i.e., capable of both); a needle is not included. It is intended for various medical applications and is not dedicated to medication administration. At the distal end of the barrel is a male connector (typically Luer-lock/slip type) for the attachment to a hypodermic needle or an administration set. It is typically made of plastic and silicone materials and may have anti-stick plunger allowing smooth plunger movement, either manually or by a syringe pump. This is a single-use device.

Regulatory Flags#

DUNS number
527035248
Device count
1
Lot or batch
true
Manufacturing date on label
true
Expiration date on label
true
No natural rubber latex
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
06934841570009TKMDTKSN2020-09-16
06934841570016TKMDTKSN2020-11-05
06934841570023TKMDTKSN2020-11-05
06934841570030TKMDTKSN2020-11-12
06934841570047TKMDTKSN2020-11-12
06934841570054TKMDTKSN2020-11-12
06934841570061TKMDTKSN2020-11-12
06934841570078TKMDTKSN2020-11-12
06934841570085TKMDTKSN2020-11-12
06934841570092TKMDTKSN2021-02-04
06934841570108TKMDTKSN2021-02-04
06934841570115TKMDTKSN2021-02-04
06934841570122TKMDTKSN2021-02-04
06934841570139TKMDTKSN2021-02-04
06934841570146TKMDTKSN2021-02-04
06934841570153TKMDTKSN2021-02-04
06934841570160TKMDTKSN2021-02-04
06934841570177TKMDTKSN2021-02-04
06934841570184TKMDTKSN2021-02-04
06934841570191TKMDTKSN2021-02-04

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Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
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18257200121083O-GENESISOrthofix US LLCFMF2026-07-17
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