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Hacs-A25-2(c)

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 4879Model HACS-A15-1,HACS-A15-2,HACS-A15-3,HACS-A15-4,HACS-A15-5,HACS-A20-1,HACS-A20-2,HACS-A20-3,HACS-A20-4,HACS-A20-5,HACS-A25-1,HACS-A25-2,HACS-A25-3,HACS-A25-4,HACS-A25-5

by Shining 3D Tech Co., Ltd.

Identity

Trade Name
HACS-A25-2(C) EUDAMED
SHINING 3D® FDA UDI
Generic Name
Dental implant abutment analog, laboratory FDA UDI
Model / Reference
HACS-A15-1,HACS-A15-2,HACS-A15-3,HACS-A15-4,HACS-A15-5,HACS-A20-1,HACS-A20-2,HACS-A20-3,HACS-A20-4,HACS-A20-5,HACS-A25-1,HACS-A25-2,HACS-A25-3,HACS-A25-4,HACS-A25-5 EUDAMED
4879 EUDAMED
HACS-A25-2(C) FDA UDI

Identifiers

Primary DI / UDI-DI
06970163084879 EUDAMEDFDA UDI
Basic UDI-DI
697016308ScanbodyNP EUDAMED
Direct Marketing DI
06970163084879 EUDAMED
FDA Product Code
NDP FDA UDI
EMDN Code
Q0199 ODONTOLOGY DEVICES - OTHER EUDAMED
GMDN Term
Dental implant abutment analog, laboratory FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
872.3980 FDA UDI
Market of Registration
Netherlands EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

Yes

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

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Hacs-A25-2(c) by Shining 3D Tech Co., Ltd. — 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

EUDAMED SRN
CN-MF-000008402
Authorised Representative
Lotus NL B.V. NL-AR-000000121

Sources (2)

  • EUDAMED 63305ca8-96d2-4630-bdd5-3d9a288c7392 61 fields · synced Jun 19, 2026
  • FDA UDI 448fcf62-a8ac-4599-b487-ec38c5d82c9d 32 fields · synced May 29, 2026