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Led Curing Light

EUDAMEDFDA UDIFDA 510(k)

Class I (EU MDR)

Ref G1Ref G8Ref G6(B)Ref G5Ref G7

by Foshan Cicada Dental Instrument Co., Ltd

Identity

Trade Name
Led Curing Light EUDAMED
CICADA FDA UDI
Generic Name
Dental laboratory curing unit FDA UDI
Device Name
Led Curing Light EUDAMED
Curing Light FDA UDI
Model / Reference
G1 EUDAMED
G8 EUDAMED
G6(B) EUDAMED
G5 EUDAMED
G7 EUDAMED
CV-215-G1 FDA UDI
Description
Curing Light FDA UDI

Identifiers

Primary DI / UDI-DI
06974456210044 EUDAMEDFDA UDI
06974456210457 EUDAMED
06974456210426 EUDAMED
06974456210396 EUDAMED
06974456210433 EUDAMED
Basic UDI-DI
697445621G1ZJ EUDAMED
697445621G823 EUDAMED
697445621G6(B)99 EUDAMED
697445621G5ZS EUDAMED
697445621G7ZW EUDAMED
510(k) Number
K192233 FDA UDI
FDA Product Code
EBZ FDA UDI
EMDN Code
L159099 ODONTOSTOMATOLOGY INSTRUMENTS, REUSABLE - OTHER EUDAMED
GMDN Term
Dental laboratory curing unit FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
872.6070 FDA UDI
Market of Registration
France 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

EUDAMEDEUDAMED

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Led Curing Light by Foshan CICADA Dental Instrument Co., Ltd. — Class I — FDA_510K, MDR — listed in EUDAMED, FDA GUDID, FDA 510(k)

Authorization Coverage (2 countries)

Regulatory Authorizations

United States Active

FDA_510K

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CN-MF-000001167
Authorised Representative
Lotus NL B.V. NL-AR-000000121

Sources (7)

  • EUDAMED 45b37a95-d0c5-4811-b517-9eebf80a97ba 61 fields · synced Jul 23, 2026
  • FDA UDI cafed764-3f6a-49bc-a664-b1355554a6ae 34 fields · synced May 30, 2026
  • EUDAMED d2117e19-17e6-4fb8-849e-7a7e5ce33e20 61 fields · synced Jun 18, 2026
  • EUDAMED e46925e9-2109-4733-8453-0dc924f92db7 61 fields · synced Jul 11, 2026
  • EUDAMED 0a8b7abb-31dc-4177-83b6-d776cc11b883 61 fields · synced Jul 15, 2026
  • EUDAMED 567483af-07b4-459e-9d65-8b496fd7e786 61 fields · synced Jul 21, 2026
  • FDA 510(k) K192233 1 fields · synced May 18, 2026