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Integra® Miltex®

FDA UDI

Class II (US FDA UDI)

by Integra LifeSciences Production Corporation

Identity

Trade Name
Integra® Miltex® FDA UDI
Generic Name
Pelvic-organ-supporting pessary FDA UDI
Device Name
Integra® Miltex® PESSARY RING SIZE 1 WITHOUT SUPPORT FDA UDI
Model / Reference
30-R1 FDA UDI
Description
Integra® Miltex® PESSARY RING SIZE 1 WITHOUT SUPPORT FDA UDI

Identifiers

Catalog Number
30-R1 FDA UDI
Primary DI / UDI-DI
10381780171409 FDA UDI
510(k) Number
K013289 FDA UDI
FDA Product Code
HHW FDA UDI
GMDN Term
Pelvic-organ-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

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Pelvic-organ-supporting pessary

Integra® Miltex® by Integra LifeSciences Production Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pelvic-organ-supporting pessary.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI bba0c443-01f3-4622-8b8d-0aafd55751a1 37 fields · synced Jun 9, 2026