EndoVive Standard PEG Kit

GUDID 08714729296805

Percutaneous Endoscopic Gastrostomy Kit

BOSTON SCIENTIFIC CORPORATION

Gastrostomy tube kit, medicated
Primary Device ID08714729296805
NIH Device Record Keydbede213-9e44-4a2e-b1a3-b0dc4f8b9724
Commercial Distribution StatusIn Commercial Distribution
Brand NameEndoVive Standard PEG Kit
Version Model NumberM00568250
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
GS108714729296805 [Package]
Contains: 08714729748717
Package: [2 Units]
In Commercial Distribution
GS108714729748717 [Primary]

FDA Product Code

KNTTUBES, GASTROINTESTINAL (AND ACCESSORIES)

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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