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Dental Surgical Instrument

EUDAMEDFDA UDI

Class I (EU MDR)

Ref KBT001

by Cowellmedi Co., Ltd.

Identity

Trade Name
Dental Surgical Instrument EUDAMED
Dental Surgical Kit FDA UDI
Generic Name
Dental/maxillofacial surgical procedure kit, non-medicated, reusable FDA UDI
Device Name
COWELL BMP Trephine Kit EUDAMED
Model / Reference
KBT001 EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
08809471726554 EUDAMEDFDA UDI
Basic UDI-DI
B-08809471726554 EUDAMED
FDA Product Code
NDP FDA UDI
EMDN Code
L159016 DENTAL SURGERY INSTRUMENT KITS, REUSABLE EUDAMED
GMDN Term
Dental/maxillofacial surgical procedure kit, non-medicated, 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

Category: Dental/maxillofacial surgical procedure kit, non-medicated, reusable

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

Similar devices

Also classified as Dental/maxillofacial surgical procedure kit, non-medicated, reusable.

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 af1b5e33-ecd9-4296-9e04-6d84c309903d 61 fields · synced Jun 19, 2026
  • FDA UDI 8a5a424e-a2ea-4186-8633-8a8869304b51 32 fields · synced May 30, 2026