← Back to catalogue

IH Transfer Impression Coping

EUDAMEDFDA UDI

Class I (EU MDR)

Ref AIHTIMH4014

by SEWONMEDIX Inc.

Identity

Trade Name
IH Transfer Impression Coping EUDAMEDFDA UDI
Generic Name
Dental implant suprastructure, permanent, preformed FDA UDI
Device Name
IH IMPLANT SYSTEM / Laboratory components & Etc. EUDAMED
SEWON MEDIX IH Transfer Impression Coping Mini Hex Set Product, Ø4.0x14.6mm FDA UDI
Model / Reference
AIHTIMH4014 EUDAMEDFDA UDI
Description
SEWON MEDIX IH Transfer Impression Coping Mini Hex Set Product, Ø4.0x14.6mm FDA UDI

Identifiers

Catalog Number
AIHTIMH4014 FDA UDI
Primary DI / UDI-DI
08800041352807 EUDAMEDFDA UDI
Basic UDI-DI
8800041300003014W EUDAMED
510(k) Number
K153521 FDA UDI
FDA Product Code
NHA FDA UDI
EMDN Code
P01020101 DENTAL IMPLANTS EUDAMED
GMDN Term
Dental implant suprastructure, permanent, preformed FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
872.3630 FDA UDI
Market of Registration
Poland 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Stent Diameter — 4.80 Millimeter FDA UDI

IH Transfer Impression Coping by SEWONMEDIX Inc. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
SEWONMEDIX Inc.
EUDAMED SRN
KR-MF-000016194
Authorised Representative
Advena Limited MT-AR-000000234

Sources (2)

  • EUDAMED b1bbe9e4-8aa2-478a-adf9-210152b0023a 61 fields · synced Jun 18, 2026
  • FDA UDI 86a368bf-cc14-462e-b03f-41b8df579f4c 38 fields · synced May 30, 2026