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Medline

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline FDA UDI
Generic Name
Bladder-supporting pessary FDA UDI
Device Name
PESSARY, CUBE, W/O DRAIN, SIZE 10, 75MM FDA UDI
Model / Reference
MDS6300310 FDA UDI
Description
PESSARY, CUBE, W/O DRAIN, SIZE 10, 75MM FDA UDI

Identifiers

Catalog Number
MDS6300310 FDA UDI
Primary DI / UDI-DI
10888277630581 FDA UDI
FDA Product Code
HHW FDA UDI
GMDN Term
Bladder-supporting pessary 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

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: Bladder-supporting pessary

A comprehensive medical device directory listing for the Medline Pessary, a non-invasive solution for female urinary incontinence and bladder prolapse. This device is designed to support the urethra/bladder neck/bladder.

Similar devices

Also classified as Bladder-supporting pessary.

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
Medline Industries, Inc.

Sources (1)

  • FDA UDI 24188af5-7917-4645-aabd-1ce01c939f13 35 fields · synced Jul 18, 2026