PROMEPLA S.A.M
Complaint File Establishment per 21 CFR 820.198; Develop Specifications But Do Not Manufacture At This Facility; Manufac | Monaco Monaco-Ville | Monaco
Verification
- Yes: Official registry Listed in openFDA device registration and listing (active manufacturers, sterilizers).
- Yes: Registration or licence number Record no. 3006617533 (issued by the source registry).
- No: Cross-source match Not found in another source.
- No: Website verified Website not checked.
Reputability score 60 of 100. A data-completeness and verification score, not a rating or endorsement. How it works
Details
- IndustryHub facility ID
- openfda:3006617533
- Category
- Medical disposables
- Sector
- Complaint File Establishment per 21 CFR 820.198; Develop Specifications But Do Not Manufacture At This Facility; Manufac
- Activity
- Catheter, Irrigation; Device, Cystometric, Hydraulic; Dislodger, Stone, Flexible; Injector, Contrast Medium, Automatic; Lithotriptor, Electro-Hydraulic; Lithotriptor, Ultrasonic; Microtools, Assisted Reproduction (Pipettes), Exempt; Needle,
- Location
- Monaco Monaco-Ville, Monaco
- Country
- Monaco
Data source
openFDA device registration and listing (active manufacturers, sterilizers). Licence: US government work, public domain (CC0).
Listings are not endorsements. IndustryHub does not verify, vet or vouch for any business. Buyers must do their own due diligence, confirm licences and certifications, and follow all export, import and sanctions laws.
