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Hayden Medical

FDA UDI

Class II (US FDA UDI)

by Hayden Medical Inc

Identity

Trade Name
Hayden Medical FDA UDI
Generic Name
Vaginal dilator FDA UDI
Device Name
Flexible Silicone Vaginal Dilator (medium) Set, Vaginal-Rectal, set of 4 FDA UDI
Model / Reference
PDS-B FDA UDI
Description
Flexible Silicone Vaginal Dilator (medium) Set, Vaginal-Rectal, set of 4 FDA UDI

Identifiers

Catalog Number
PDS-B FDA UDI
Primary DI / UDI-DI
00840319733622 FDA UDI
510(k) Number
K130273 FDA UDI
FDA Product Code
HDX FDA UDI
GMDN Term
Vaginal dilator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.3900 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

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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Vaginal dilator

Hayden Medical by Hayden Medical Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vaginal dilator.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hayden Medical Inc

Sources (1)

  • FDA UDI 71c43731-cbe9-4c5e-aa13-5a288655c9c3 36 fields · synced May 31, 2026