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MU ScanBody

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref DSMUSBLFSModel DENTIS Implant Surgical Instrument SystemRef DSMUSBLRef DSMUSBLF

by Dentis Co. , Ltd

Identity

Trade Name
MU ScanBody EUDAMEDFDA UDI
s-Clean MU Scanbody FDA UDI
Generic Name
Dental implant abutment analog, intraoral-scanning, single-use FDA UDI
Device Name
DENTIS Implant Surgical Instrument System EUDAMED
MU ScanBody (DSMUSBLFS) FDA UDI
MU ScanBody (DSMUSBLF) FDA UDI
Dental Implant Instrument / s-Clean MU Scanbody FDA UDI
Model / Reference
DSMUSBLFS EUDAMEDFDA UDI
DSMUSBLF EUDAMEDFDA UDI
DSMUSBL EUDAMEDFDA UDI
DENTIS Implant Surgical Instrument System EUDAMED
Description
MU ScanBody (DSMUSBLFS) FDA UDI
MU ScanBody (DSMUSBLF) FDA UDI
Dental Implant Instrument / s-Clean MU Scanbody FDA UDI

Identifiers

Primary DI / UDI-DI
08800266941084 EUDAMEDFDA UDI
08800266941183 EUDAMEDFDA UDI
08800053040419 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 abutment analog, intraoral-scanning, single-use 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 abutment analog, intraoral-scanning, single-use

MU ScanBody 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 abutment analog, intraoral-scanning, single-use.

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 (6)

  • FDA UDI 2b9691d2-80a8-4259-8aae-2e6e2b63c861 33 fields · synced Jul 30, 2026
  • FDA UDI 5f393dab-8568-415d-8336-cb746ac350ac 33 fields · synced May 30, 2026
  • FDA UDI b9148ed1-f124-487f-b4dd-bccbb9d6f55e 33 fields · synced May 30, 2026
  • EUDAMED 98e9a0ef-4c7a-4044-9695-62ce7bd7bc97 61 fields · synced Jul 13, 2026
  • EUDAMED 8c511222-b1e0-4031-9cf8-64a9c6a0351b 61 fields · synced Jul 21, 2026
  • EUDAMED d6637adb-e441-4c9a-a2e3-517d0674b391 61 fields · synced Jul 30, 2026