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Aquarius

FDA UDI

Class II (US FDA UDI)

by Degania Silicone Ltd

Identity

Trade Name
Aquarius FDA UDI
Generic Name
Enteral tube extension, single-use FDA UDI
Device Name
Feeding Set 30cm E.Set ENFit feed & straight conn. FDA UDI
Model / Reference
1032430080AQ FDA UDI
Description
Feeding Set 30cm E.Set ENFit feed & straight conn. FDA UDI

Identifiers

Primary DI / UDI-DI
07290001609828 FDA UDI
FDA Product Code
KNT FDA UDI
PIF FDA UDI
GMDN Term
Enteral tube extension, single-use 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

No

FDA UDI

Contains Latex

No

FDA UDI

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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Enteral tube extension, single-use

Aquarius by Degania Silicone Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Enteral tube extension, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 533a075c-8340-4c93-b42f-cb12e7420208 33 fields · synced Jun 1, 2026