Screw cap.134GD BRAUN BIO.VD VZ50

GUDID 04038917989640

Screw cap.134GD BRAUN BIO.VD VZ50

Sarstedt Aktiengesellschaft & Co.KG

Test tube/reservoir cap IVD Test tube/reservoir cap IVD Test tube/reservoir cap IVD Test tube/reservoir cap IVD Test tube/reservoir cap IVD Test tube/reservoir cap IVD Test tube/reservoir cap IVD Test tube/reservoir cap IVD Test tube/reservoir cap IVD Test tube/reservoir cap IVD Test tube/reservoir cap IVD Test tube/reservoir cap IVD Test tube/reservoir cap IVD Test tube/reservoir cap IVD Test tube/reservoir cap IVD Test tube/reservoir cap IVD Test tube/reservoir cap IVD
Primary Device ID04038917989640
NIH Device Record Keycb687b9b-8428-498b-83f2-bdfea7b5a3df
Commercial Distribution StatusIn Commercial Distribution
Brand NameScrew cap.134GD BRAUN BIO.VD VZ50
Version Model Number65.716.229
Company DUNS388000270
Company NameSarstedt Aktiengesellschaft & Co.KG
Device Count50
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
GS104038917989640 [Unit of Use]
GS104038917989657 [Primary]

FDA Product Code

KDTContainer, Specimen Mailer And Storage, Sterile

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-02-28
Device Publish Date2024-02-20

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