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s-Clean Transfer Impression Coping

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref DSTLZModel DENTIS Implant Surgical Instrument System

by Dentis Co. , Ltd

Identity

Trade Name
s-Clean Transfer Impression Guide Pin EUDAMED
s-Clean Transfer Impression Coping FDA UDI
Generic Name
Dental implant suprastructure, temporary, preformed, single-use FDA UDI
Device Name
DENTIS Implant Surgical Instrument System EUDAMED
Dental Implant Instrument / s-Clean Transfer Impression Coping FDA UDI
Model / Reference
DSTLZ EUDAMEDFDA UDI
DENTIS Implant Surgical Instrument System EUDAMED
Description
Dental Implant Instrument / s-Clean Transfer Impression Coping FDA UDI

Identifiers

Primary DI / UDI-DI
08800053014656 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 suprastructure, temporary, preformed, 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 suprastructure, temporary, preformed, single-use

s-Clean Transfer Impression Coping 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 suprastructure, temporary, preformed, 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 (2)

  • FDA UDI b1664613-52ba-4f03-836a-9aa2daed8072 33 fields · synced Jul 9, 2026
  • EUDAMED 6431efc1-a64d-47a1-a1d0-02f3635c9ac3 61 fields · synced Jul 9, 2026