Medistri SA
Domdidier Fribourg, CH
MEDISTRI SA appears in FDA device records in Domdidier Fribourg, CH. FDA records list no 510(k) clearances, no PMA records and one registered establishment. As of , FDA records show no recalls for this company, and at least one establishment registration is current.
FDA records held for this company
- 510(k) clearances
- 0
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 1
510(k) clearance history
No 510(k) clearance records for this company in the ingested FDA data.
No 510(k) clearance records in the ingested FDA data.
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 3006946276 | 3006946276 | MEDISTRI SA | Route de l'industrie, 96, Domdidier Fribourg 1564 CH | 2026 | and 34 more, listed in full below |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
- SDQAlfapump System
- HRXArthroscope
- HMXCannula, Ophthalmic
- KRACatheter, Continuous Flush
- DQYCatheter, Percutaneous
- MCWCatheter, Peripheral, Atherectomy
- LOXCatheters, Transluminal Coronary Angioplasty, Percutaneous
- NDNCement, Bone, Vertebroplasty
- JDQCerclage, Fixation
- FRODressing, Wound, Drug
- PRCDrug-Coated Peripheral Transluminal Angioplasty Catheter
- ONUDrug-Eluting Peripheral Transluminal Angioplasty Catheter
- SDDElectromechanical Surgical System Wherein The Surgeon Annd The User Interface Can Be In The Sterile Field
- MAIFastener, Fixation, Biodegradable, Soft Tissue
- MBIFastener, Fixation, Nondegradable, Soft Tissue
- MSSFolders And Injectors, Intraocular Lens (Iol)
- HQEInstrument, Vitreous Aspiration And Cutting, Ac-Powered
- HQLIntraocular Lens
- KYBLens, Guide, Intraocular
- OWXMesh, Surgical, Non-Absorbable, Orthopaedics, Reinforcement Of Tendon
- HRMMicroscope, Operating & Accessories, Ac-Powered, Ophthalmic
- OOEOphthalmic Femtosecond Laser
- PBFOrthopaedic Surgical Planning And Instrument Guides
- SBFOrthopedic Augmented Reality
- QEWPeripheral Mechanical Thrombectomy With Aspiration
- JDKProsthesis, Hip, Cement Restrictor
- KWZProsthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer
- KWYProsthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented
- LZOProsthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented
- LPHProsthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
- MEHProsthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate
- KROProsthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer
- HSXProsthesis, Knee, Femorotibial, Non-Constrained, Cemented, Metal/Polymer
- KRRProsthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer
- JWHProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
- HSDProsthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented
- KWSProsthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented
- MBFProsthesis, Shoulder, Semi-Constrained, Metal/Polymer, Uncemented
- PHXShoulder Prosthesis, Reverse Configuration
- NIPStent, Superficial Femoral Artery
- GATSuture, Nonabsorbable, Synthetic, Polyethylene
- HQCUnit, Phacofragmentation
- HTNWasher, Bolt Nut
- DQXWire, Guide, Catheter
Recall records
No recall records for this company in the ingested FDA data.
Verification record
There is no verification record for this company. Most companies on this site have none: a record exists only where a company asked to be verified and MDM ran the checks, so the absence of one says nothing about the company.
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Data as of , FDA export datePage updated Source: openFDA, public domain