Medicel AG
⚠️ Moderate Risk
FEI: 1000581837 • Altenrhein, Saint Gall • SWITZERLAND
FEI Number
1000581837
Location
Altenrhein, Saint Gall
Country
SWITZERLANDAddress
Dornierstrasse 11, , Altenrhein, Saint Gall, Switzerland
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
How is this score calculated?
Proprietary Algorithm
- 40% Violation Severity — AI-assessed (1-10)
- 30% Refusal Volume — Logarithmic scale
- 20% Recency — Decays over 5 years
- 10% Frequency — Refusals per year
© ImportRefusal.com Original Analysis
Violation Summary
NOT LISTED
It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).
FRNMFGREG
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.
REGISTERED
It appears the device is subject to listing under 510(j) and the initial distributor has not registered as required by 21 CFR 807.20 (a)(5).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 8/31/2023 | 86MSSFOLDERS AND INJECTORS, INTRAOCULAR LENS (IOL) | Division of West Coast Imports (DWCI) | |
| 1/18/2023 | 86KYGDEVICE, IRRIGATION, OCULAR SURGERY | Division of Southeast Imports (DSEI) | |
| 12/19/2022 | 79NAYSYSTEM, SURGICAL, COMPUTER CONTROLLED INSTRUMENT | 118NOT LISTED | Division of Southeast Imports (DSEI) |
| 9/29/2021 | 87JDXINSTRUMENT, SURGICAL, SONIC AND ACCESSORY/ATTACHMENT | 118NOT LISTED | Division of Southeast Imports (DSEI) |
| 5/27/2021 | 86HQLLENS, INTRAOCULAR | 118NOT LISTED | Division of Southeast Imports (DSEI) |
| 5/27/2021 | 86HQLLENS, INTRAOCULAR | 118NOT LISTED | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is Medicel AG's FDA import refusal history?
Medicel AG (FEI: 1000581837) has 6 FDA import refusal record(s) in our database, spanning from 5/27/2021 to 8/31/2023.
What is an FEI number?
FEI stands for Firm Establishment Identifier. It's a unique number assigned by the FDA to identify establishments that manufacture, process, pack, or hold food, drugs, medical devices, or other FDA-regulated products. Medicel AG's FEI number is 1000581837.
What types of violations has Medicel AG received?
Medicel AG has been cited for 3 different violation type(s). Common FDA violations include adulteration (unsafe or unsanitary products), misbranding (incorrect or misleading labels), and regulatory non-compliance.
Where does this information about Medicel AG come from?
All FDA import refusal data for Medicel AG is sourced from the official FDA Data Dashboard (datadashboard.fda.gov), a public government database maintained by the U.S. Food and Drug Administration.
Data sourced from the FDA Data Dashboard, a public database maintained by the U.S. Food and Drug Administration.