Mobility+ Enteral Feeding Device 1900 mm

FDA UDI

Class II (US FDA UDI)

by Rockfield Medical Devices Limited

Identity

Trade Name: Mobility+ Enteral Feeding Device 1900 mm FDA UDI
Generic Name: Enteral feeding noninvasive-component set FDA UDI
Device Name: The Mobility+ Enteral Feeding System (“Mobility+ System”) is a portable, lightweight, non-electronic, disposable enteral feeding system intended to deliver commercially available liquid nutrition formula to a patient, using a standard extension set (or feeding tube) with an ENFit® connector, in the clinical or home care settings. FDA UDI
Model / Reference: MOB2-1900 FDA UDI
Description: The Mobility+ Enteral Feeding System (“Mobility+ System”) is a portable, lightweight, non-electronic, disposable enteral feeding system intended to deliver commercially available liquid nutrition formula to a patient, using a standard extension set (or feeding tube) with an ENFit® connector, in the clinical or home care settings. FDA UDI

Identifiers

Catalog Number: MOB2-1900-30, MOB2-1900-03,MOB2-1900-03-09, MOB2-1900-10, MOB2-1900-10-03 FDA UDI
Primary DI / UDI-DI: 05391537090158 FDA UDI
510(k) Number: K233034 FDA UDI
FDA Product Code: PIF FDA UDI
KNT FDA UDI
GMDN Term: Enteral feeding noninvasive-component set 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Dimensions & Sizes

Size: Length — 1900 Millimeter FDA UDI

Category: Enteral feeding noninvasive-component set

Mobility+ Enteral Feeding Device 1900 mm by Rockfield Medical Devices Limited — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Cleared under the same submission

K233034 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Rockfield Medical Devices Limited

Sources (1)

FDA UDI 13a06cb6-bbec-4147-b6b7-14008779da0f 36 fields · synced May 31, 2026