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Euro-Med

FDA UDI

Class I (US FDA UDI)

by CooperSurgical, Inc.

Identity

Trade Name
EURO-MED FDA UDI
Generic Name
Open-surgery biopsy forceps, reusable FDA UDI
Device Name
EuroMed handle for rotating punch tips FDA UDI
Model / Reference
64-649 FDA UDI
Description
EuroMed handle for rotating punch tips FDA UDI

Identifiers

Primary DI / UDI-DI
00888937017304 FDA UDI
FDA Product Code
HFB FDA UDI
GMDN Term
Open-surgery biopsy forceps, 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Open-surgery biopsy forceps, reusable

Euro-Med by CooperSurgical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Open-surgery biopsy forceps, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6e6bbf95-5945-441c-a112-e1c783c2dc76 33 fields · synced Jun 9, 2026