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Lat 4mm Straight Curette

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 287354655

by Avalign Technologies Inc.

Identity

Trade Name
Depuy Synthes FDA UDI
Generic Name
Bone curette, reusable FDA UDI
Device Name
LAT 4MM STRAIGHT CURETTE EUDAMED
LAT 6MM ANGLED DOWN-BITING CURETTE, LEFT FDA UDI
Model / Reference
287354655 EUDAMEDFDA UDI
Description
LAT 6MM ANGLED DOWN-BITING CURETTE, LEFT FDA UDI

Identifiers

Primary DI / UDI-DI
00190776152864 EUDAMEDFDA UDI
Basic UDI-DI
0190776SCRAPVZ EUDAMED
Direct Marketing DI
00190776152864 EUDAMED
FDA Product Code
HTF FDA UDI
EMDN Code
L0901 ORTHOPAEDIC SURGERY SPOONS AND CURETTES, REUSABLE EUDAMED
GMDN Term
Bone curette, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
878.4800 FDA UDI
Market of Registration
Bulgaria EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Bone curette, reusable

Lat 4mm Straight Curette by AVALIGN TECHNOLOGIES, Inc. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone curette, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
US-MF-000008511
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (2)

  • EUDAMED e81f7d25-30ca-47a3-8e45-4f44b386f2f4 61 fields · synced Jul 29, 2026
  • FDA UDI f61a357d-799a-4a50-b0ad-6692c10736b9 34 fields · synced May 30, 2026