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Sonata® IUUS Probe Soaking Cylinder

FDA UDI

Class II (US FDA UDI)

by Gynesonics, Inc.

Identity

Trade Name
Sonata® IUUS Probe Soaking Cylinder FDA UDI
Generic Name
General laboratory container, reusable FDA UDI
Device Name
General laboratory container, reusable FDA UDI
Model / Reference
CYL-001 FDA UDI
Description
General laboratory container, reusable FDA UDI

Identifiers

Catalog Number
CYL-001 FDA UDI
Primary DI / UDI-DI
10817929020142 FDA UDI
FDA Product Code
IYO FDA UDI
ITX FDA UDI
KNF FDA UDI
GMDN Term
General laboratory container, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1560 FDA UDI
892.1570 FDA UDI
884.4160 FDA UDI
Commercial Distribution
Not 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

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Sonata® IUUS Probe Soaking Cylinder by Gynesonics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Gynesonics, Inc.

Sources (1)

  • FDA UDI e7c4baa1-a346-40ce-b1b2-e12b21bf68ab 36 fields · synced May 31, 2026