Eu Mdd Eu Md Class 3 On The Market 🇰🇷 South Korea

LuciFill VOLUME

BioPlus Co., Ltd. · 🇰🇷 South Korea
Devices (same UDI-DI)
1
Certificates
1
Countries
2
Notified Bodies
1

Basic Information

Primary DI
08809947980503
Basic UDI-DI Code
B-08809947980503
Reference
BPLN-60
Device Types
Single use Sterile
Regulation
Eu Mdd
Classification
Eu Md Class 3
Status
On The Market
Manufacturer
BioPlus Co., Ltd.

Additional Description

LuciFill VOLUME consists of stabilized, hyaluronic acid (HA) formulated to a concentration of 2%(20mg/1ml). Hyaluronic acid based dermal filler composed of small particles intended for facial tissue augmentation by injection into skin layer. LuciFill VOLUME is a transparent, viscous and sterile gel, supplied in a disposable pre- filled syringe. The contents of the syringe are sterile. The syringe is equipped with a plunger stopper, finger grip and plunger rod. Needles are on the outside of the blister package, and they are placed in a sterile condition in the packaging box.

CND Nomenclature Codes

Code Description
P900402 RESORBABLE FILLING AND RECONSTRUCTION DEVICES

Certificates

Type Number
MDD Annex II Section 4 2195-MED-1418802

Available In Countries

🇩🇪 Germany 🇹🇷 Türkiye

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