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Endosee Advance Cannula with Pipet

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref ESPX5

by CooperSurgical, Inc.

Identity

Trade Name
Endosee® Advance System EUDAMED
Endosee Advance Cannula with Pipet FDA UDI
Generic Name
Intrauterine cannula, single-use FDA UDI
Device Name
Endosee® Advance System EUDAMED
Endosee Advance Cannula with Pipet - 1 Kit - Contains - 1 Cannula and 1 Pipet Curet Endometrial Suction Curette 3mm OD FDA UDI
Model / Reference
ESPX5 EUDAMEDFDA UDI
Description
Endosee Advance Cannula with Pipet - 1 Kit - Contains - 1 Cannula and 1 Pipet Curet Endometrial Suction Curette 3mm OD FDA UDI

Identifiers

Primary DI / UDI-DI
60888937022003 EUDAMEDFDA UDI
Basic UDI-DI
0888937TD008ns34 EUDAMED
FDA Product Code
FAJ FDA UDI
HIH FDA UDI
EMDN Code
Z12020785 GENITOURINARY ENDOSCOPY INSTRUMENTS - CONSUMABLES EUDAMED
GMDN Term
Intrauterine cannula, single-use FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
876.1500 FDA UDI
884.1690 FDA UDI
Market of Registration
Netherlands EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

Category: Intrauterine cannula, single-use

Endosee Advance Cannula with Pipet by CooperSurgical, Inc. — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Intrauterine cannula, single-use.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI 515be586-0eeb-4632-8f2e-7ba32c1cbfb6 33 fields · synced Jun 18, 2026
  • EUDAMED 34e84faf-23dd-43a3-a62d-b4e85096c6a5 61 fields · synced Jun 18, 2026