FDA Registration Active 🇳🇱 Netherlands

27G Chandelier fiber and 23G standard D-style fiber optic handpiece incl. guidance needle.

Reg #: 9611516 · FEI: 3002806863 · Expires 2025
Products
1
Proprietary Names
15
Establishment Types
2
Classifications
1

Registration Details

Registration Name
D.O.R.C. Dutch Ophthalmic Research Center (International) B.V.
Registration Number
9611516
FEI Number
3002806863
Status
Active
Expiry Year
2025
Initial Importer
No
Address
SCHEIJDELVEWEG 2
City
ZUIDLAND Zuid-Holland
Country
NL

Regulatory Submissions

510(k) Number
K062895

Owner / Operator

Firm Name
D.O.R.C. Dutch Ophthalmic Research Center (International) B.
Operator Number
8030460
Address
SCHEIJDELVEWEG 2, --
City
ZUIDLAND
State
Zuid-Holland
Postal Code
3214 VN
Country
NL
Correspondent
Michel - van der Schans

US Agent

Business Name
Dutch Ophthalmic USA
Contact Name
Deborah Thibodeaux
Address
10 Continental Drive, Bldg 1
City
Exeter
State
NH
ZIP
03833
Country
US
Phone
603 7786929 ext. 170

Products

Device Name Product Code
Endoilluminator MPA

Proprietary Names

27G Chandelier fiber and 23G standard D-style fiber optic handpiece incl. guidance needle. Endoillumination Probe, including illuminated scleral depressor TotalView Chandelier for Eckardt cannula system Spare bulb for REF: 1266.XIII Xenon BrightStar illumination System. Shielded TotalView Endoillumination Probe, including illuminated scleral depressor Disposable Chandelier fiber (one fiber) incl. guidance needle TotalView Endoillumination Probe, with 2 exchangeable tips Extendible Light Probe Disposable Chandelier fiber (one fiber) with Photon connector and guidance needle TotalView Chandelier for cannula system Spaide TotalView Endoillumination Probe, including illuminated scleral depressor Disposable Eckardt Twinlight Chandelier TotalView Endoillumination Probe, including illuminated scleral depressor Combined 23G Eckardt Multi-Fiber Endoillumination Probe / Chandelier Eckardt TwinLight Chandelier with Photon connector and guidance needle

Establishment Types

Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device