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EndoVive Jejunal Feeding Tube

FDA UDI

Class II (US FDA UDI)

by Boston Scientific

Identity

Trade Name
EndoVive Jejunal Feeding Tube FDA UDI
Generic Name
Gastrojejunostomy tube FDA UDI
Device Name
3-Port Through-the-PEG J-Tube Kit FDA UDI
Model / Reference
M00566320 FDA UDI
Description
3-Port Through-the-PEG J-Tube Kit FDA UDI

Identifiers

Primary DI / UDI-DI
08714729786313 FDA UDI
FDA Product Code
KNT FDA UDI
FPD FDA UDI
GMDN Term
Gastrojejunostomy tube 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

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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: Gastrojejunostomy tube

EndoVive Jejunal Feeding Tube by Boston Scientific — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Gastrojejunostomy tube.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Boston Scientific

Sources (1)

  • FDA UDI 40006d4f-cd44-4f85-b370-e36f4a73c333 34 fields · synced Jun 8, 2026