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Caya contoured diaphragm

FDA UDI

Class II (US FDA UDI)

by KESSEL medintim GmbH

Identity

Trade Name
Caya contoured diaphragm FDA UDI
Generic Name
Diaphragm pessary FDA UDI
Device Name
Caya Silicone Vaginal Diaphragm for contraception FDA UDI
Model / Reference
Caya contoured diaphragm FDA UDI
Description
Caya Silicone Vaginal Diaphragm for contraception FDA UDI

Identifiers

Catalog Number
DIA CAYA USA FDA UDI
Primary DI / UDI-DI
04013273001649 FDA UDI
510(k) Number
K140305 FDA UDI
FDA Product Code
HDW FDA UDI
GMDN Term
Diaphragm pessary FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.5350 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Diaphragm pessary

Caya contoured diaphragm by KESSEL medintim GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Diaphragm pessary.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
KESSEL medintim GmbH

Sources (1)

  • FDA UDI 2f61e32f-6e04-4c37-a6e7-5a5761c04996 38 fields · synced Jun 6, 2026