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Anatomic Colours

EUDAMEDFDA UDI

Class I (EU MDR)

Ref DB377R

by Aesculap AG

Identity

Trade Name
ANATOMIC COLOURS EUDAMEDFDA UDI
Generic Name
Periodontal curette FDA UDI
Device Name
Dental curette/scaler EUDAMED
MC CALL ANATOMIC COLOURS Universal Curette, curved, 6 1/2", (165 mm), double ended, ergonomic handle, peek handle, Fig. M17S/18S, black, non-sterile, reusable FDA UDI
Model / Reference
DB377R EUDAMEDFDA UDI
Description
MC CALL ANATOMIC COLOURS Universal Curette, curved, 6 1/2", (165 mm), double ended, ergonomic handle, peek handle, Fig. M17S/18S, black, non-sterile, reusable FDA UDI

Identifiers

Catalog Number
DB377R FDA UDI
Primary DI / UDI-DI
04038653146659 EUDAMEDFDA UDI
Basic UDI-DI
40392390000018102H EUDAMED
FDA Product Code
EMK FDA UDI
EMDN Code
L159001 DENTAL AND PERIODONTAL CURETTES, REUSABLE EUDAMED
GMDN Term
Periodontal curette FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
872.4565 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

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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Anatomic Colours by Aesculap AG — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Aesculap AG
EUDAMED SRN
DE-MF-000005504

Sources (2)

  • EUDAMED a5f2eed1-5d56-40cf-8945-d8897334939f 61 fields · synced May 30, 2026
  • FDA UDI 070a5bf0-423b-4bb7-975b-15899b53b2da 35 fields · synced May 30, 2026