Miser™
Miser™: 10 catalogue numbers listed by Merit Medical Systems, Inc., United States, under Set, Administration, Intravascular. 49 manufacturers in China are registered for this product code.
49manufacturers in China registered for this device type
10catalogue numbers in this listing
3510(k) clearances naming this product code
9recalls on this code
Who Else Makes It
Concentrated in Zhejiang (12), Jiangsu (11), Shanghai (10). 13 of them are registered as contract manufacturers, able to build to a buyer’s own specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Promisemed Hangzhou Meditech Co., Ltd. | Hangzhou | Zhejiang | Contract manufacturer | 21 |
| Hantech Medical Device Co., Ltd. | Cixi | Zhejiang | Contract manufacturer | 18 |
| Forefront Medical Technology (Jiangsu) Co., Ltd. | Changzhou | Jiangsu | Contract manufacturer | 14 |
| BQ Plus Medical Co., Ltd. | Songjiang | Shanghai | Contract manufacturer | 13 |
| Ningbo Tianyi Medical Appliance Co., Ltd. | Ningbo | Zhejiang | Contract manufacturer | 11 |
| Anhui Tiankang Medical Technology Co., Ltd. | Tianchang | Anhui | Contract manufacturer | 9 |
| Anhui Kangda Medical Products Co., Ltd. | Tianchang | Anhui | Contract manufacturer | 7 |
| JDI Electronics Factory | Dongguan | Guangdong | Contract manufacturer | 7 |
| Yangzhou Xingwei Medical Technology Co., Ltd. | Yangzhou | Jiangsu | Contract manufacturer | 5 |
| Wenzhou K.L.F. Medical Plastics Co., Ltd. | Wenzhou | Zhejiang | Contract manufacturer | 4 |
| Advance Technology Ltd | Shenzhen | Guangdong | Contract manufacturer | 3 |
| Weihai Jierui Medical Products Co., Ltd. | Weihai | Shandong | Contract manufacturer | 3 |
Showing 12 of 49. All 49 manufacturers in China registered for Set, Administration, Intravascular
Record
| Listed by | Merit Medical Systems, Inc., United States |
|---|---|
| FDA product code | FPA |
| Device type | Set, Administration, Intravascular |
| Device class | Class 2 |
| Regulation | 21 CFR 880.5440 |
| Establishment | Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter |
| Record published | 2025-08-14 |
| Record revised | 2025-05-12 (version 7) |
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 |
| Packaging | Pack of 10 |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| D | Tubing Length (in/cm)-2″ (5.1 cm) | In distribution |
| C | Tubing Length (in/cm)-72″ (183 cm) | In distribution |
| 00884450099896 | Tubing Length (in/cm)-72″ (183 cm) | In distribution |
| 00884450014226 | Tubing Length (in/cm)-72″ (183 cm) | In distribution |
| C | Tubing Length (in/cm)-72″ (183 cm) | In distribution |
| C | Tubing Length (in/cm)-72″ (183 cm) | In distribution |
| 00884450109120 | Tubing Length (in/cm)-2″ (5.1 cm) | In distribution |
| 00884450116982 | Tubing Length (in/cm)-72″ (183 cm) | In distribution |
| 00884450014219 | Tubing Length (in/cm)-72″ (183 cm) | In distribution |
| C | Tubing Length (in/cm)-72″ (183 cm) | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| ICU Medical | ICU Medical, Inc | 529 |
| Codan | Codan US Corp. | 510 |
| Vygon | Vygon Corp. | 355 |
| Port Access Needle | Bard Access Systems, Inc. | 341 |
| Set, Administration, Intravascular | Mps Medical, Inc. | 291 |
| Alaris, SmartSite | BD Switzerland Sàrl | 266 |
| IV Administration Set | B. Braun Medical Inc. | 242 |
| Medex | ICU Medical, Inc | 237 |
| Extension Set | B. Braun Medical Inc. | 171 |
| MaxGuard | BD Switzerland Sàrl | 150 |
| Medline | Medline Industries, Inc. | 148 |
| Centurion | Centurion Medical Products Corporation | 145 |
Showing 12 of 768. All products under Set, Administration, Intravascular
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K083576 | 2008-12-23 |
| K961794 | 1996-08-01 |
| K915678 | 1992-07-30 |
Recalls
1 of these is Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.
| Initiated | FDA class | Root cause | Reason | Quantity | Closed |
|---|---|---|---|---|---|
| 2016-08-12 | Class II | Component design/selection | Merit Medical Systems, Inc. announces a voluntary field action for Fluid Administration Sets due to a molding defect in the drip chamber. | 107,341 total devices | 2017-05-09 |
| 2008-04-08 | Not classified | Mixed-up of materials/components | Convenience kits may contain non-filtered drip chambers | 64 kits | 2009-04-06 |
| 2008-04-08 | Not classified | Mixed-up of materials/components | Convenience kits may contain non-filtered drip chambers | 55 kits | 2009-04-06 |
| 2008-04-08 | Not classified | Mixed-up of materials/components | Convenience kits may contain non-filtered drip chambers | 102 kits | 2009-04-06 |
| 2008-04-08 | Not classified | Mixed-up of materials/components | Convenience kits may contain non-filtered drip chambers | 95 kits | 2009-04-06 |
| 2008-04-08 | Not classified | Mixed-up of materials/components | Convenience kits may contain non-filtered drip chambers | 113 kits | 2009-04-06 |
| 2008-04-08 | Not classified | Mixed-up of materials/components | Convenience kits may contain non-filtered drip chambers | 217 kits | 2009-04-06 |
| 2008-04-08 | Not classified | Mixed-up of materials/components | Convenience kits may contain non-filtered drip chambers. | 99 kits | 2009-04-06 |
| 2008-04-08 | Not classified | Mixed-up of materials/components | Convenience kits may contain non-filtered drip chambers | 120 kits | 2009-04-06 |
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.