VentiSure2
26 catalogue numbers from 301-5812, listed by Engineered Medical Systems, LLC, United States, under Ventilator, Emergency, Manual (Resuscitator). 8 manufacturers in China are registered for this product code.
8manufacturers in China registered for this device type
26catalogue numbers in this listing
6510(k) clearances naming this product code
Who Else Makes It
Concentrated in Fujian (4), Zhejiang (1), Guangdong (1). 5 of them are registered as contract manufacturers, able to build to a buyer’s own specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Flexicare Medical (Dongguan) Ltd. | Dongguan | Guangdong | Contract manufacturer | 48 |
| GaleMed (Xiamen) Co., Ltd. | Xiamen | Fujian | Contract manufacturer | 33 |
| Polymed (Xiamen) Plastic Industrial Co., Ltd. | Xiamen | Fujian | Contract manufacturer | 17 |
| VR Medical Technology Co., Ltd. | Kunshan | Jiangsu | Contract manufacturer | 13 |
| Ambu Limited | Xiang Yu F.T.Z., Xiamen | Fujian | Contract manufacturer | 11 |
| Huzhou Junda Industry Co., Ltd. | Anji | Zhejiang | Contract manufacturer | 129 |
| Laerdal Medical (Suzhou) Co., Ltd. | 215009 Suzhou Jiangsu Province | Repacker / relabeller | 12 | |
| Xiamen Compower Medical Tech. Co., Ltd. | Xiamen | Fujian | Contract manufacturer | 9 |
Record
| Listed by | Engineered Medical Systems, LLC, United States |
|---|---|
| FDA product code | BTM |
| Device type | Ventilator, Emergency, Manual (Resuscitator) |
| Device class | Class 2 |
| Regulation | 21 CFR 868.5915 |
| Establishment | Contract manufacturer, Manufacturer |
| Record published | 2016-10-30 |
| Record revised | 2019-11-11 (version 4) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Single use | Yes |
| Prescription | Prescription only |
| Label carries | lot or batch number, expiry date |
| Packaging | Pack of 8, pack of 16 |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 301-5812 | Adult | In distribution |
| 301-5736 | Pediatric | In distribution |
| 301-5740 | Adult | In distribution |
| 301-5737 | Infant | In distribution |
| 301-5800 | Pediatric | In distribution |
| 301-5735 | Adult | In distribution |
| 301-5734 | Large Adult | In distribution |
| 301-5911 | Neo/Infant | In distribution |
| 301-5803 | Adult | In distribution |
| 301-5678 | Pediatric | In distribution |
| 301-5581 | Adult | In distribution |
| 301-5810 | Adult | In distribution |
| 301-5811 | Large Adult | In distribution |
| 301-5802 | Adult | In distribution |
| 301-5742 | Adult | In distribution |
| 301-5726 | Pediatric | In distribution |
| 301-5818 | Pediatric | In distribution |
| 301-5817 | Infant | In distribution |
| 301-5680 | Large Adult | In distribution |
| 301-5677 | Infant | In distribution |
| 301-5580 | Pediatric | In distribution |
| 301-5579 | Infant | In distribution |
| 301-5739 | Large Adult | In distribution |
| 301-5813 | Large Adult | In distribution |
| 301-5679 | Adult | In distribution |
| 301-5582 | Large Adult | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Ventlab | Ventlab, LLC | 405 |
| CPR-2 Bag | Mercury Medical Enterprises, LLC | 231 |
| CPR Bag | Mercury Medical Enterprises, LLC | 187 |
| Vital Signs™ | Airlife, Inc. | 102 |
| Medline | Medline Industries, Inc. | 78 |
| Spur® II Pediatric ResuscitatorSingle Patient Use Resuscitator | Ambu A/S | 74 |
| Spur® II Adult ResuscitatorSingle Patient Use Resuscitator | Ambu A/S | 66 |
| Hudson RCI | Teleflex Medical LLC | 56 |
| Medline Industries, Inc. | Medline Industries, Inc. | 53 |
| Portex | ICU Medical, Inc | 45 |
| Spur® II Infant ResuscitatorSingle Patient Use Resuscitator | Ambu A/S | 45 |
| Curaplex® | Bound Tree Medical, LLC | 38 |
Showing 12 of 342. All products under Ventilator, Emergency, Manual (Resuscitator)
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K991955 | 1999-07-06 |
| K991953 | 1999-07-01 |
| K932797 | 1993-09-03 |
| K924671 | 1993-04-21 |
| K924610 | 1993-04-06 |
| K912203 | 1991-11-13 |
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.