← Back to catalogue

EndoVive Low Profile Replacement Button

FDA UDI

Class II (US FDA UDI)

by Boston Scientific

Identity

Trade Name
EndoVive Low Profile Replacement Button FDA UDI
Generic Name
Enteral feeding kit, adult/paediatric, sterile FDA UDI
Device Name
Low Profile Replacement Gastrostomy Tube FDA UDI
Model / Reference
M00562760 FDA UDI
Description
Low Profile Replacement Gastrostomy Tube FDA UDI

Identifiers

Primary DI / UDI-DI
08714729284017 FDA UDI
FDA Product Code
KNT 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 Low Profile Replacement 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Boston Scientific

Sources (1)

  • FDA UDI 30574bce-fda4-4889-84ed-1b182bb77ca7 34 fields · synced May 30, 2026