FDA.reportPublic FDA data

EndoVive Standard PEG Kit

Primary DI
08714729285205
Brand
EndoVive Standard PEG Kit
Company
BOSTON SCIENTIFIC CORPORATION
Model
M00568210
Device description
Percutaneous Endoscopic Gastrostomy Kit
Published
2016-09-24
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
true
Single use
true

Product Codes#

Code, Name table
CodeName
KNTTUBES, GASTROINTESTINAL (AND ACCESSORIES)

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
KNTTubes, Gastrointestinal (And Accessories)Gastroenterology, Urology2

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
08714729285205PackageGS12In Commercial Distribution
08714729748694PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
08714729285205087147292852058714729285205
08714729748694087147297486948714729748694

GMDN Terms#

Term, Definition table
TermDefinition
Gastrostomy tube kit, medicatedA collection of devices which includes a gastrostomy tube with a pharmaceutical agent intended for short- and/or long-term (= 24 hours) access to the stomach via a gastrostomy. In addition to the gastrostomy tube and pharmaceutical agent, the kit might also include additional surgical devices (e.g., scalpel, introduction needle, guidewire, dilator, fastener, lubricant). This is a single-use device.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Device Size Text, specify0
Device Size Text, specify0

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
021717889
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
true
Combination product
true
Lot or batch
true
Serial number
false
Manufacturing date on label
false
Expiration date on label
true
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
08714729749172RX Cholangiogram KitM005714802016-09-24
00191506020729iNod™ Ultrasound Guided Biopsy NeM00502060M005020602023-03-21
00191506020910iNod™ Ultrasound Guidance ConsoM00503210M005032102023-03-21
00191506020927iNod™ Ultrasound Guidance ConsoM0050321R0M0050321R02023-03-21
00191506020934iNod™M00503300M005033002023-03-21
00191506020941iNod™M0050330R0M0050330R02023-03-21
00191506021924iNod™M00503200M005032002023-03-21
00191506021931iNod™M0050320R0M0050320R02023-03-21
08714729860853Expel™ Drainage Catheter with Twist-Loc™ HubH74939341082502016-08-17
08714729860860Expel™ Drainage Catheter with Twist-Loc™ HubH74939341102502016-08-17
08714729860877Expel™ Drainage Catheter with Twist-Loc™ HubH74939341122502016-08-17
08714729860884Expel™ Drainage Catheter with Twist-Loc™ HubH74939341142502016-08-17
08714729860891Expel™ Drainage Catheter with Twist-Loc™ HubH749393410825K12016-08-17
08714729860907Expel™ Drainage Catheter with Twist-Loc™ HubH749393411025K12016-08-17
08714729860914Expel™ Drainage Catheter with Twist-Loc™ HubH749393411225K12016-08-17
00802526623400NA694669462024-08-29
00802526604430INGEVITY™+78402020-02-06
00802526604522INGEVITY™+78422020-02-06
00802526604577INGEVITY™+78412020-02-06
00802526480546NA662866282014-09-24

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Primary DI, Brand, Company table
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