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Pipelle®

FDA UDI

Class II (US FDA UDI)

by Laboratoire Ccd

Identity

Trade Name
PIPELLE® FDA UDI
Generic Name
Cervical cytology brush FDA UDI
Device Name
Device for endometrial sampling FDA UDI
Model / Reference
PIPELLE® FDA UDI
Description
Device for endometrial sampling FDA UDI

Identifiers

Catalog Number
1103000 FDA UDI
Primary DI / UDI-DI
03700111400719 FDA UDI
FDA Product Code
HHK FDA UDI
GMDN Term
Cervical cytology brush FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.1175 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Catheter Length — 23.5 Centimeter FDA UDI
Outer Diameter — 0.31 Centimeter FDA UDI

Category: Cervical cytology brush

Pipelle® by Laboratoire Ccd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cervical cytology brush.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Laboratoire Ccd

Sources (1)

  • FDA UDI ba1bbd58-1334-4937-b96d-037c5f27b9ac 37 fields · synced May 30, 2026