Millex-GV
2 catalogue numbers from SLGVM33RS, listed by Merck Millipore Ltd., Ireland, under Filter, Conduction, Anesthetic. 1 manufacturer in China is registered for this product code.
1manufacturer
2catalogue numbers in this listing
1510(k) clearance
Who Else Makes It
Registered in Zhejiang. One is registered as a contract manufacturer, able to build to a specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Zhejiang Runqiang Medical Instruments Co., Ltd. | Jiaxing | Zhejiang | Contract manufacturer | 9 |
Record
| Listed by | Merck Millipore Ltd., Ireland |
|---|---|
| FDA product code | BSN |
| Device type | Filter, Conduction, Anesthetic |
| Device class | Class 2 |
| Regulation | 21 CFR 868.5130 |
| Establishment | Manufacturer |
| Premarket notification | Exempt |
| Record published | 2016-09-22 |
| Record revised | 2023-05-15 (version 5) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Supplied sterile | Yes |
| Single use | Yes |
| Prescription | Prescription only |
| Label carries | lot or batch number, expiry date, manufacturing date |
Catalogue Numbers
| Catalogue number | Size | Per pack | Status |
|---|---|---|---|
| SLGVM33RS | 50 | In distribution | |
| SLGV013SL | 100 | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Dash 6 | Gbuk Group Limited | 8 |
| Portex | ICU Medical, Inc | 6 |
| Millex-HV | Merck Millipore Ltd. | 3 |
| Filter | Pajunk Gmbh Medizintechnologie | 3 |
| Millex-OR | Merck Millipore Ltd. | 2 |
| Millex-HA | Merck Millipore Ltd. | 2 |
| Millex-FG | Merck Millipore Ltd. | 2 |
| Millex-MP | Merck Millipore Ltd. | 2 |
| Millex-GS | Merck Millipore Ltd. | 2 |
| Filter NRFit | Pajunk Gmbh Medizintechnologie | 1 |
| Millex-HP | Merck Millipore Ltd. | 1 |
| Vented Millex-AA | Merck Millipore Ltd. | 1 |
Showing 12 of 22. All products under Filter, Conduction, Anesthetic
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K133004 | 2014-03-27 |
Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.