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s-Clean MU Straight Abutment Digital Lap

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref DSMUSDLModel DENTIS Implant Surgical Instrument System

by Dentis Co. , Ltd

Identity

Trade Name
MU Straight Abutment Digital Lab EUDAMED
s-Clean MU Straight Abutment Digital Lap FDA UDI
Generic Name
Dental implant analog FDA UDI
Device Name
DENTIS Implant Surgical Instrument System EUDAMED
Dental Implant Instrument / s-Clean MU Straight Abutment Digital Lap FDA UDI
Model / Reference
DSMUSDL EUDAMEDFDA UDI
DENTIS Implant Surgical Instrument System EUDAMED
Description
Dental Implant Instrument / s-Clean MU Straight Abutment Digital Lap FDA UDI

Identifiers

Primary DI / UDI-DI
08800053033626 EUDAMEDFDA UDI
Basic UDI-DI
88061691DENTIS-I7L EUDAMED
FDA Product Code
NDP FDA UDI
EMDN Code
P01020180 DENTAL IMPLANTS - ACCESSORIES EUDAMED
GMDN Term
Dental implant analog FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
872.3980 FDA UDI
Market of Registration
Spain EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental implant analog

s-Clean MU Straight Abutment Digital Lap by Dentis Co. , Ltd — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Dental implant analog.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dentis Co. , Ltd

Sources (2)

  • FDA UDI 94a42738-a7b4-4c24-9659-afaca7a52592 33 fields · synced Jul 23, 2026
  • EUDAMED a4e92f26-a109-4220-825b-c876af61146e 61 fields · synced Jul 23, 2026