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Emerge

EUDAMEDFDA UDI

Class IIb (EU MDR)

Ref 0500-0001Model 0500-0001

by Cynosure LLC

Identity

Trade Name
Emerge EUDAMEDFDA UDI
Generic Name
Dermatological diode laser system FDA UDI
Device Name
Emerge EUDAMED
Emerge Laser Assembly FDA UDI
Model / Reference
0500-0001 EUDAMEDFDA UDI
Description
Emerge Laser Assembly FDA UDI

Identifiers

Primary DI / UDI-DI
00841494100179 EUDAMEDFDA UDI
Basic UDI-DI
B-00841494100179 EUDAMED
510(k) Number
K111840 FDA UDI
FDA Product Code
ONG FDA UDI
EMDN Code
Z12011016 DIODE SURGICAL LASER EUDAMED
GMDN Term
Dermatological diode laser system FDA UDI

Classification

Device Class
Class IIb EUDAMED
Class II FDA UDI
Regulation Number
878.4810 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

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Emerge by Cynosure, LLC — 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

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Manufacturer

Manufacturer
Cynosure LLC
EUDAMED SRN
US-MF-000010200
Authorised Representative
Cynosure B.V. NL-AR-000009566

Sources (2)

  • EUDAMED 0e7fe638-c382-40f6-9ef2-6bf324f44776 61 fields · synced Jun 20, 2026
  • FDA UDI 816dbca9-1003-4acd-a312-8cdb11863148 34 fields · synced May 30, 2026