← Back to catalogue

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 3 FDA UDI
Model / Reference
UR203 FDA UDI
Description
Uresta Bladder Support Size 3 FDA UDI

Identifiers

Catalog Number
UR203 FDA UDI
Primary DI / UDI-DI
00692379000219 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Resilia, Inc.

Sources (1)

  • FDA UDI 846d13dd-c814-4a1e-bc52-c0ce4e72d33d 35 fields · synced May 30, 2026