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e-Clean Transfer Impression Guide Pin

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref DETSWModel DENTIS Implant Surgical Instrument System

by Dentis Co. , Ltd

Identity

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

Identifiers

Primary DI / UDI-DI
08806169142825 EUDAMEDFDA UDI
08806169142801 FDA 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

e-Clean Transfer Impression Guide Pin 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 (3)

  • FDA UDI 4c4da3e6-a663-47cc-aaae-9b815127d547 33 fields · synced Jul 23, 2026
  • FDA UDI ea6fc089-36f1-478e-b805-411b7a1553f7 33 fields · synced May 30, 2026
  • EUDAMED 7a7860f7-19a0-4f4c-90ce-428ceb8fbc39 61 fields · synced Jul 23, 2026