Home › GRI Medical & Electronic Technology Co., Ltd. › Alleset
Alleset
GRI Medical & Electronic Technology Co., Ltd. · Model 49-OMRTK01 · UDI-DI 16931918177984
10
510(k) clearances
69
Adverse events
2
Recalls
584
Facilities
Description
New issued for UMiami RTOK_0MRTK01_ATC_Lift sheet_Armboard cover_ Bags_strap_mophead_Non-sterile_12ea/cs
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2023-06-23 | Microtek Medical Inc. | Certain lots of the products have a Naphthalene odor. |
| 2017-12-27 | LITTLE RAPIDS CORPORATION | The secondary supplier provided material was within specification but did not meet our design needs compared to the primary manufacturer. The product is designed for patient trans |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.