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Tubo Estensione 150 Cm- Nutrifit

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 368.1572

by Pentaferte Italia Srl

Identity

Trade Name
TUBO ESTENSIONE 150 CM- NUTRIFIT EUDAMED
NUTRIFIT FDA UDI
Generic Name
Enteral tube extension, single-use FDA UDI
Device Name
TUBI ED ACCESSORI PER ALIMENTAZIONE ENTERALE EUDAMED
EXTENSION TUBE 150cm, for enteral use FDA UDI
Model / Reference
368.1572 EUDAMEDFDA UDI
Description
EXTENSION TUBE 150cm, for enteral use FDA UDI

Identifiers

Primary DI / UDI-DI
08015262035662 EUDAMEDFDA UDI
Basic UDI-DI
80152621064Y EUDAMED
FDA Product Code
FPD FDA UDI
KNT FDA UDI
EMDN Code
A03020199 EXTENSIONS - OTHER EUDAMED
GMDN Term
Enteral tube extension, single-use FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
876.5980 FDA UDI
Market of Registration
Italy EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

Yes

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Tubo Estensione 150 Cm- Nutrifit by Pentaferte Italia Srl — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
IT-MF-000040982

Sources (2)

  • EUDAMED e4b0406b-3dce-40e8-9f65-846e5d04cecc 61 fields · synced Oct 6, 2026
  • FDA UDI 56021f22-5607-4438-a076-96b84b8951ba 33 fields · synced May 30, 2026