hypodermic needles

GUDID 06949236202526

Berpu Medical Technology Co.,Ltd

Hypodermic needle, single-use
Primary Device ID06949236202526
NIH Device Record Key4cbc6be3-8023-4ef1-af86-c2df6aa33b0e
Commercial Distribution StatusIn Commercial Distribution
Brand Namehypodermic needles
Version Model Number25G×25mmRW
Company DUNS529239746
Company NameBerpu Medical Technology Co.,Ltd
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
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
GS106949236202519 [Primary]
GS106949236202526 [Package]
Contains: 06949236202519
Package: [100 Units]
In Commercial Distribution
GS106949236202533 [Package]
Package: [40 Units]
In Commercial Distribution

FDA Product Code

FMINeedle, Hypodermic, Single Lumen

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-10-20
Device Publish Date2020-10-12

On-Brand Devices [hypodermic needles]

0694923620231130G×13mmRW
0694923620234223G×38mmTW
0694923620252625G×25mmRW
0694923620249625G×38mmRW
0694923620246522G×38mmTW
0694923620243421G×38mmTW
0694923620240320G×38mmTW
0694923620237319G×38mmTW

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