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Dental Instrument

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 2SSFIGP14

by Cowellmedi Co., Ltd.

Identity

Trade Name
Dental Instrument EUDAMEDFDA UDI
Generic Name
Dental implant suprastructure reamer guide FDA UDI
Device Name
Guide Pin EUDAMED
Model / Reference
2SSFIGP14 EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
08800016144468 EUDAMEDFDA UDI
Basic UDI-DI
B-08800016144468 EUDAMED
FDA Product Code
NDP FDA UDI
EMDN Code
L80 SURGICAL INSTRUMENTS, REUSABLE - VARIOUS ACCESSORIES EUDAMED
GMDN Term
Dental implant suprastructure reamer guide 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

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Manufacturer

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

Sources (2)

  • EUDAMED 57fbc46e-fb8f-4f60-ae1a-6f2b33aef0cc 61 fields · synced Jul 13, 2026
  • FDA UDI 550b61dc-baca-44fc-a82f-8c9fcc1b2c67 32 fields · synced May 30, 2026