← Back to catalogue

Dental Instrument

EUDAMEDFDA UDI

Class I (EU MDR)

Ref KSFR3819L

by Cowellmedi Co., Ltd.

Identity

Trade Name
Dental Instrument EUDAMEDFDA UDI
Generic Name
Surgical screwdriver, reusable FDA UDI
Device Name
SFIT Absolute Ratchet Driver EUDAMED
Model / Reference
KSFR3819L EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
08800016111705 EUDAMEDFDA UDI
Basic UDI-DI
B-08800016111705 EUDAMED
FDA Product Code
NDP FDA UDI
EMDN Code
L80 SURGICAL INSTRUMENTS, REUSABLE - VARIOUS ACCESSORIES EUDAMED
GMDN Term
Surgical screwdriver, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
872.3980 FDA UDI
Market of Registration
Netherlands 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

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dental Instrument by Cowellmedi Co., Ltd — Class I — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

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

Manufacturer

EUDAMED SRN
KR-MF-000009689
Authorised Representative
AR Experts B.V. NL-AR-000023989

Sources (2)

  • EUDAMED 1b659966-f393-459d-b487-9d07c2ee10fb 61 fields · synced May 30, 2026
  • FDA UDI 9c94f6e6-c776-4084-a864-df98cba025f9 32 fields · synced May 30, 2026