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Uresta®

FDA UDI

Class II (US FDA UDI)

by Resilia, Inc.

Identity

Trade Name
Uresta® FDA UDI
Generic Name
Urinary-incontinence vaginal insert, reusable FDA UDI
Device Name
Uresta Bladder Support Size 4 FDA UDI
Model / Reference
UR204 FDA UDI
Description
Uresta Bladder Support Size 4 FDA UDI

Identifiers

Catalog Number
UR204 FDA UDI
Primary DI / UDI-DI
00692379000226 FDA UDI
FDA Product Code
HHW FDA UDI
GMDN Term
Urinary-incontinence vaginal insert, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.3575 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

Yes

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Urinary-incontinence vaginal insert, reusable

Uresta® by Resilia, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Urinary-incontinence vaginal insert, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Resilia, Inc.

Sources (1)

  • FDA UDI 4ce45e5b-daa2-404a-aa9a-4c1014baa7bf 35 fields · synced Jun 6, 2026