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Healing Abutment

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref CI 3606Model STERILE COMPONENTS

by S.I.N. - Sistema DE Implante Nacional S.A.

Identity

Trade Name
HEALING CAP HE Ø3.6XØ5.0X6MM EUDAMED
Healing Abutment FDA UDI
Generic Name
Dental implant suprastructure, temporary, preformed, single-use FDA UDI
Device Name
HEALING CAP EUDAMED
HEALING CAP EXT HEX Ø 3,6 X 5,0 X 6MM FDA UDI
Model / Reference
CI 3606 EUDAMEDFDA UDI
STERILE COMPONENTS EUDAMED
Description
HEALING CAP EXT HEX Ø 3,6 X 5,0 X 6MM FDA UDI

Identifiers

Catalog Number
CI 3606 FDA UDI
Primary DI / UDI-DI
07899995205605 EUDAMEDFDA UDI
Basic UDI-DI
999520000057KB EUDAMED
510(k) Number
K170398 FDA UDI
FDA Product Code
NHA FDA UDI
EMDN Code
P01020180 DENTAL IMPLANTS - ACCESSORIES EUDAMED
GMDN Term
Dental implant suprastructure, temporary, preformed, single-use FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
872.3630 FDA UDI
Market of Registration
Portugal EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dental implant suprastructure, temporary, preformed, single-use

Healing Abutment by S.I.N. - Sistema DE Implante Nacional S.A. — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Dental implant suprastructure, temporary, preformed, single-use.

Cleared under the same submission

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI 698a3289-a435-4822-a629-85cefb21742b 35 fields · synced Jun 18, 2026
  • EUDAMED ff4f9d2f-dc5c-41b4-8119-4e51bc0cf1a4 61 fields · synced Jun 18, 2026