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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,MRLND,WO SUPPRT,SZ 4, 2.75",70MM FDA UDI
Model / Reference
MDS6301304 FDA UDI
Description
PESSARY,MRLND,WO SUPPRT,SZ 4, 2.75",70MM FDA UDI

Identifiers

Catalog Number
MDS6301304 FDA UDI
Primary DI / UDI-DI
10888277631441 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

Medline by Medline Industries, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bladder-supporting pessary.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medline Industries, Inc.

Sources (1)

  • FDA UDI 65e7ccd7-ad80-4396-8254-4ae26d1897ec 35 fields · synced Jun 1, 2026