IDryNeedle 0.30x50

GUDID 28809407787059

Feeltech Co.,Ltd.

Acupuncture needle, single-use Acupuncture needle, single-use Acupuncture needle, single-use Acupuncture needle, single-use Acupuncture needle, single-use Acupuncture needle, single-use Acupuncture needle, single-use Acupuncture needle, single-use Acupuncture needle, single-use Acupuncture needle, single-use Acupuncture needle, single-use Acupuncture needle, single-use
Primary Device ID28809407787059
NIH Device Record Keyf52c0e85-c8f4-476b-ba1a-62f36cd036b4
Commercial Distribution StatusIn Commercial Distribution
Brand NameIDryNeedle 0.30x50
Version Model NumberDN150 0.30x50
Company DUNS688432407
Company NameFeeltech Co.,Ltd.
Device Count100
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 Datefalse
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
GS108809407787055 [Unit of Use]
GS118809407787052 [Primary]
GS128809407787059 [Package]
Contains: 18809407787052
Package: Cartonbox [20000 Units]
In Commercial Distribution
GS138809407787056 [Package]
Package: CARTONBOX [20000 Units]
In Commercial Distribution

FDA Product Code

MQXNeedle, Acupuncture, Single Use

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-01-23
Device Publish Date2020-01-15

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