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Diaphragm Valve Fill Tube and Reflux Valve

FDA UDI

Class III (US FDA UDI)

by Allergan

Identity

Trade Name
Diaphragm Valve Fill Tube and Reflux Valve FDA UDI
Generic Name
Saline-filled breast implant, unstructured FDA UDI
Device Name
Diaphragm Valve Fill Tube & Reflux Valve FDA UDI
Model / Reference
25-00017 FDA UDI
Description
Diaphragm Valve Fill Tube & Reflux Valve FDA UDI

Identifiers

Catalog Number
25-00017 FDA UDI
Primary DI / UDI-DI
10888628006287 FDA UDI
FDA Product Code
FTR FDA UDI
GMDN Term
Saline-filled breast implant, unstructured FDA UDI

Classification

Device Class
Class III FDA UDI
Regulation Number
878.3540 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
MRI Safety
MR Safe FDA UDI

Category: Saline-filled breast implant, unstructured

Diaphragm Valve Fill Tube and Reflux Valve by Allergan — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Saline-filled breast implant, unstructured.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Allergan

Sources (1)

  • FDA UDI a77689ee-9968-4e07-b068-228b54e4365d 35 fields · synced May 30, 2026