← Back to catalogue
IH Temporary Abutment
EUDAMEDFDA UDIClass IIb (EU MDR)
Ref AIHTAMH4010Model IH IMPLANT SYSTEM
Identity
- Trade Name
- IH Temporary Abutment EUDAMEDFDA UDI
- Generic Name
- Dental implant suprastructure, temporary, preformed, single-use FDA UDI
- Device Name
- IH Temporary Abutment EUDAMEDSEWON MEDIX IH Temporary Abutment Mini Hex Non-Coating Set Product, Ø4.0x1.0mm FDA UDI
- Model / Reference
- IH IMPLANT SYSTEM EUDAMEDAIHTAMH4010 EUDAMEDFDA UDI
- Description
- SEWON MEDIX IH Temporary Abutment Mini Hex Non-Coating Set Product, Ø4.0x1.0mm FDA UDI
Identifiers
- Catalog Number
- AIHTAMH4010 FDA UDI
- Primary DI / UDI-DI
- 08800041350513 EUDAMEDFDA UDI
- Basic UDI-DI
- B-08800041350513 EUDAMED
- 510(k) Number
- K153521 FDA UDI
- FDA Product Code
- NHA FDA UDI
- EMDN Code
- P01020101 DENTAL IMPLANTS EUDAMED
- GMDN Term
- Dental implant suprastructure, temporary, preformed, single-use FDA UDI
Classification
- Device Class
- Class IIb EUDAMEDClass 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
Yes
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
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
IH Temporary Abutment by SEWONMEDIX Inc. — Class IIb — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDD
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-08800041350513 | Class IIb | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIb | Pending data |
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 4d60f10e-7473-4baf-b09e-c113b2c56fc0 61 fields · synced Jul 9, 2026
- FDA UDI a68dd740-c898-4f5f-b437-9e44ca02f5ff 35 fields · synced May 30, 2026