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Dil-Os Cervical Dilator/Uterine Sound

FDA UDI

Class I (US FDA UDI)

by CooperSurgical, Inc.

Identity

Trade Name
Dil-Os Cervical Dilator/Uterine Sound FDA UDI
Generic Name
Uterine sound, reusable FDA UDI
Device Name
Dil-Os Cervical Dilator/Uterine Sound- Slight Curve FDA UDI
Model / Reference
64-336 FDA UDI
Description
Dil-Os Cervical Dilator/Uterine Sound- Slight Curve FDA UDI

Identifiers

Primary DI / UDI-DI
00888937017786 FDA UDI
FDA Product Code
HDQ FDA UDI
GMDN Term
Uterine sound, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
884.4530 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

Yes

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

Dimensions & Sizes

Size
Length — 323 Millimeter FDA UDI

Category: Uterine sound, reusable

Dil-Os Cervical Dilator/Uterine Sound by CooperSurgical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Uterine sound, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d0c0b285-9510-4918-b565-61fb6b5f8d01 34 fields · synced Jun 9, 2026