← Back to catalogue

Powers Double Bent Curette Straight

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 5190-S

by Innomed, Inc.

Identity

Trade Name
Powers Double Bent Curette Straight EUDAMED
Innomed, Inc. FDA UDI
Generic Name
Bone curette, reusable FDA UDI
Device Name
Curette EUDAMED
Powers Double Bent Curette Straight FDA UDI
Model / Reference
5190-S EUDAMEDFDA UDI
Description
Powers Double Bent Curette Straight FDA UDI

Identifiers

Catalog Number
5190-S FDA UDI
Primary DI / UDI-DI
00840277123534 EUDAMEDFDA UDI
Basic UDI-DI
8402771INNOCURET01ZB EUDAMED
Direct Marketing DI
00840277123534 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
Germany 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

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

No

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

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

Powers Double Bent Curette Straight by Innomed, 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Innomed, Inc.
EUDAMED SRN
US-MF-000014761
Authorised Representative
MediMark Europe Sarl. FR-AR-000000182

Sources (2)

  • EUDAMED 1b3f265c-d138-4821-92a6-261c95c2dcd9 61 fields · synced Jul 11, 2026
  • FDA UDI 8f02114b-3b82-4a12-ae04-3bbb0092245e 34 fields · synced May 30, 2026