Torque Device for Guidewire

GUDID 06936775511530

Amsinomed Medical Co.,Ltd

Torque manipulation device Torque manipulation device Torque manipulation device Torque manipulation device Torque manipulation device Torque manipulation device Torque manipulation device Torque manipulation device Torque manipulation device Torque manipulation device Torque manipulation device Torque manipulation device Torque manipulation device Torque manipulation device
Primary Device ID06936775511530
NIH Device Record Key96e55da6-92cd-4ceb-a8c8-47f9626b3ada
Commercial Distribution StatusIn Commercial Distribution
Brand NameTorque Device for Guidewire
Version Model NumberMZCH-2-8
Company DUNS545137135
Company NameAmsinomed Medical Co.,Ltd
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS106936775511530 [Primary]

FDA Product Code

DWSInstruments, Surgical, Cardiovascular

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-04-26
Device Publish Date2023-04-18

On-Brand Devices [Torque Device for Guidewire]

06936775511585MZCH-3-12
06936775511578MZCH-3-10
06936775511561MZCH-3-8
06936775511554MZCH-2-12
06936775511547MZCH-2-10
06936775511530MZCH-2-8
06936775511523MZCH-2-5
06936775511516MZCH-1-12
06936775511509MZCH-1-10
06936775511493MZCH-1-8
06936775511486MZCH-1-5

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