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Surgical Instrument

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref CDH 0924 Model DRIVER

by S.I.N. - Sistema DE Implante Nacional S.A.

Identity

Trade Name
DRIVER DIGITAL HEX.0.9 MEDIUM EUDAMED
SURGICAL INSTRUMENT FDA UDI
Generic Name
Surgical screwdriver, single-use, non-sterile FDA UDI
Device Name
DRIVER (WITHOUT CONNECTION) EUDAMED
DRIVER HAND HEX 0.9X24 FDA UDI
Model / Reference
CDH 0924 EUDAMEDFDA UDI
DRIVER EUDAMED
Description
DRIVER HAND HEX 0.9X24 FDA UDI

Identifiers

Catalog Number
CDH 0924 FDA UDI
Primary DI / UDI-DI
07899995205070 EUDAMEDFDA UDI
Basic UDI-DI
999520000013JP EUDAMED
510(k) Number
K201688 FDA UDI
FDA Product Code
KCT FDA UDI
EMDN Code
L159099 ODONTOSTOMATOLOGY INSTRUMENTS, REUSABLE - OTHER EUDAMED
GMDN Term
Surgical screwdriver, single-use, non-sterile FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
880.6850 FDA UDI
Market of Registration
Portugal 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

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical screwdriver, single-use, non-sterile

Surgical Instrument by S.I.N. - Sistema DE Implante Nacional S.A. — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Surgical screwdriver, single-use, non-sterile.

Cleared under the same submission

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 08e1b1e1-2961-49f1-a1da-c78269215937 35 fields · synced Jul 8, 2026
  • EUDAMED 68e8bee0-17d2-4219-9724-5dc3a058a0c0 61 fields · synced Jul 8, 2026