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Papette

FDA UDI

Class II (US FDA UDI)

by CooperSurgical, Inc.

Identity

Trade Name
Papette FDA UDI
Generic Name
Uterine manipulator, single-use FDA UDI
Device Name
WALLACH Papette® (Non-Sterile) Cervical Cell Sampler FDA UDI
Model / Reference
908003 FDA UDI
Description
WALLACH Papette® (Non-Sterile) Cervical Cell Sampler FDA UDI

Identifiers

Primary DI / UDI-DI
50888937011291 FDA UDI
510(k) Number
K896065 FDA UDI
FDA Product Code
HHT FDA UDI
GMDN Term
Uterine manipulator, single-use FDA UDI

Classification

Device Class
Class II 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Uterine manipulator, single-use

Papette by CooperSurgical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Uterine manipulator, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b95de841-aea1-49e4-a085-fdb3b309b16c 34 fields · synced Jun 9, 2026