EndoVive Standard PEG Kit

GUDID 08714729880530

Percutaneous Endoscopic Gastrostomy Kit ENFit

BOSTON SCIENTIFIC CORPORATION

Gastrostomy tube kit, medicated
Primary Device ID08714729880530
NIH Device Record Key8ece0f16-3d8f-43fe-a126-985e2cc03b67
Commercial Distribution StatusIn Commercial Distribution
Brand NameEndoVive Standard PEG Kit
Version Model NumberM00509070
Company DUNS021717889
Company NameBOSTON SCIENTIFIC CORPORATION
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Producttrue
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

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Device Identifiers

Device Issuing AgencyDevice ID
GS108714729880523 [Primary]
GS108714729880530 [Package]
Contains: 08714729880523
Package: [2 Units]
In Commercial Distribution

FDA Product Code

PIFGastrointestinal Tubes with Enteral Specific Connectors

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2020-10-01
Device Publish Date2016-09-24

On-Brand Devices [EndoVive Standard PEG Kit]

08714729880530Percutaneous Endoscopic Gastrostomy Kit ENFit
08714729880516Percutaneous Endoscopic Gastrostomy Kit ENFit
08714729880493Percutaneous Endoscopic Gastrostomy Kit ENFit
08714729880479Percutaneous Endoscopic Gastrostomy Kit ENFit
08714729296805Percutaneous Endoscopic Gastrostomy Kit
08714729296799Percutaneous Endoscopic Gastrostomy Kit
08714729285205Percutaneous Endoscopic Gastrostomy Kit
08714729285199Percutaneous Endoscopic Gastrostomy Kit

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