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Endosee® Dx Cannula

FDA UDI

Class II (US FDA UDI)

by CooperSurgical, Inc.

Identity

Trade Name
Endosee® Dx Cannula FDA UDI
Generic Name
Endometrial biopsy kit FDA UDI
Device Name
Endosee® Dx Cannula FDA UDI
Model / Reference
ESDX5-SGL FDA UDI
Description
Endosee® Dx Cannula FDA UDI

Identifiers

Primary DI / UDI-DI
00888937013795 FDA UDI
510(k) Number
K132384 FDA UDI
FDA Product Code
HIH FDA UDI
GMDN Term
Endometrial biopsy kit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.1690 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

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: Endometrial biopsy kit

Endosee® Dx Cannula by CooperSurgical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endometrial biopsy kit.

Cleared under the same submission

K132384 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a7cb6f47-16ee-4215-87f8-9aef59aeec8f 34 fields · synced Jun 9, 2026