← Back to catalogue

Ss01

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 0158Model SS01

by Hangzhou SHINING3D Dental Technology Co., Ltd.

Identity

Trade Name
SS01 EUDAMED
SHINING 3D® FDA UDI
Generic Name
Dental appliance fabrication material, resin FDA UDI
Device Name
Splint Soft Resin EUDAMED
The product is used for the fabrication of preformed tooth positioner by dental professionals. FDA UDI
Model / Reference
SS01 EUDAMEDFDA UDI
0158 EUDAMED
Description
The product is used for the fabrication of preformed tooth positioner by dental professionals. FDA UDI

Identifiers

Primary DI / UDI-DI
06975338700158 EUDAMEDFDA UDI
Basic UDI-DI
697533870SS01QC EUDAMED
Direct Marketing DI
06975338700158 EUDAMED
FDA Product Code
KMY FDA UDI
EMDN Code
Q010699 MATERIALS FOR THE PREPARATION OF CUSTOM-MADE DENTAL DEVICES - OTHER EUDAMED
GMDN Term
Dental appliance fabrication material, resin FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
872.5525 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

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

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

Ss01 by Hangzhou SHINING3D Dental Technology 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-000033456
Authorised Representative
Lotus NL B.V. NL-AR-000000121

Sources (2)

  • EUDAMED 8830d1b4-b989-4e01-9b93-ca5dd289b1d6 61 fields · synced Jun 18, 2026
  • FDA UDI fefec940-991b-4676-99ca-61481abafe76 33 fields · synced May 30, 2026