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EndoVive™ One Step Button™

FDA UDI

Class II (US FDA UDI)

by Boston Scientific

Identity

Trade Name
EndoVive™ One Step Button™ FDA UDI
Generic Name
Enteral feeding kit, adult/paediatric, sterile FDA UDI
Device Name
Low Profile Percutaneous Endoscopic Gastrostomy Kit FDA UDI
Model / Reference
M00568530 FDA UDI
Description
Low Profile Percutaneous Endoscopic Gastrostomy Kit FDA UDI

Identifiers

Catalog Number
M00568530 FDA UDI
Primary DI / UDI-DI
08714729149941 FDA UDI
FDA Product Code
KGC FDA UDI
GMDN Term
Enteral feeding kit, adult/paediatric, sterile FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5980 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Enteral feeding kit, adult/paediatric, sterile

EndoVive™ One Step Button™ by Boston Scientific — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Enteral feeding kit, adult/paediatric, sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Boston Scientific

Sources (1)

  • FDA UDI cbd6f058-cb9f-4314-a929-26707e88b4ae 35 fields · synced Jun 8, 2026