FDA Registration Active 🇳🇱 Netherlands

Microforceps: End-gripping

Reg #: 9611516 · FEI: 3002806863 · Expires 2025
Products
1
Proprietary Names
26
Establishment Types
3
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

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
Forceps, Ophthalmic HNR

Proprietary Names

Microforceps: End-gripping Microforceps: Serrated Jaws Disposable Microforceps: Shah Micro Serrated Jaws Micro Capsulorhexis forceps intraocular style Disposable Microforceps: ILM Microforceps: Diamond-dusted Infusion cannula forceps Accessory: Protection cap for microforceps & microscissors. Microforceps: Asymmetrical endgripping Disposable Microforceps: Asymmetrical endgripping Forceps for removal of cannulas Disposable Microforceps: End-gripping Disposable Microforceps: Ultra peel Microforceps: ILM Scharioth IOL Scleral fixation forceps, straight & curved Scleral plug forceps Microforceps: Eckardt Power End-gripping Microforceps: Eckardt End-gripping Disposable Microforceps: Extended reach – Wide grip Microforceps: Horizontal Subretinal Disposable Microforceps: Eckardt End-gripping Microforceps: Shah Micro Serrated Jaws Microforceps: Avci Foreign Body Microforceps: High Myopic Eckardt End-gripping Akgul Biopsy Forceps with sharp tip DMEK Graft Manipulation Forceps with extra fine tips for intraocular and extraocular unrolling of the graft.

Establishment Types

Complaint File Establishment per 21 CFR 820.198 Repack or Relabel Medical Device Manufacture Medical Device