Vial Adaptor
Vial Adapter 13mm Long FLL w/25μm filter- VF 5 Pack
8manufacturers in China registered for this device type
26catalogue numbers in this listing
5510(k) clearances naming this product code
4recalls on this code
Who Else Makes It
Concentrated in Zhejiang (3), Jiangsu (3), Hong Kong (1). 3 of them are registered as contract manufacturers, able to build to a buyer’s own specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| GRI Medical & Electronic Technology Co., Ltd. | Jiaxing | Zhejiang | Contract manufacturer | 71 |
| Suzhou Jinsheng Plastic Co., Ltd. | Suzhou | Jiangsu | Contract manufacturer | 23 |
| Ming FAI Industrial (Shenzhen) Co., Ltd. | Shenzhen | Guangdong | Contract manufacturer | 17 |
| Gcmedica Enterprise Ltd.(Wuxi) | Wuxi | Jiangsu | Contract manufacturer | 55 |
| Steris Sterilization Technologies (Suzhou) Ltd | Suzhou | Jiangsu | Contract manufacturer | 44 |
| Ming FAI Enterprise International Co., Ltd. | Kowloon | Hong Kong | Exporter | 18 |
| Zhejiang Medtec Medical devices Co., Ltd. | Hangzhou | Zhejiang | Manufacturer | 10 |
| Hangzhou Qiantang Longyue Biotechnology Co., Ltd. | Hangzhou | Zhejiang | Manufacturer | 7 |
Record
| Listed by | West Pharma. Services IL, Ltd., Israel |
|---|---|
| FDA product code | LHI |
| Device type | Set, I.V. Fluid Transfer |
| Device class | Class 2 |
| Regulation | 21 CFR 880.5440 |
| Establishment | Specification developer, Manufacturer |
| 510(k) | K963583 |
| Record published | 2016-05-01 |
| Record revised | 2023-06-30 (version 8) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Sterilisation | Radiation Sterilization |
| Supplied sterile | Yes |
| Single use | Yes |
| Prescription | Prescription only |
| Label carries | lot or batch number, expiry date |
| Packaging | Pack of 4, pack of 150, pack of 1500, pack of 1300, pack of 40, pack of 432 |
| Distribution end date | 2023-06-29 |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 8070315 | In distribution | |
| 8072045 | In distribution | |
| 8070106 | In distribution | |
| 8072004 | In distribution | |
| 8070202 | In distribution | |
| 8072003 | In distribution | |
| 8070109 | In distribution | |
| 8072005 | In distribution | |
| 8070110 | In distribution | |
| 8072103 | In distribution | |
| 8072109 | In distribution | |
| 8072104 | In distribution | |
| 8072035 | In distribution | |
| 8070308 | In distribution | |
| 8070002 | In distribution | |
| 8070211 | In distribution | |
| 8072030 | In distribution | |
| 8072118 | In distribution | |
| 8072113 | In distribution | |
| 8072043 | In distribution | |
| 8070209 | In distribution | |
| 8070311 | In distribution | |
| 8070301 | Withdrawn | |
| 8072120 | Withdrawn | |
| 8070118 | Withdrawn | |
| 8072116 | Withdrawn |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Kenaflexx | Kentron Healthcare, Inc. | 49 |
| Set, I.V. Fluid Transfer | Mps Medical, Inc. | 27 |
| Vial Adapter | West Pharma. Services IL, Ltd. | 22 |
| Extension SET | MPS Pharma & Medical, Inc. | 19 |
| Vial Adapter Medic’up | Union Plastic | 17 |
| Exactamix | Baxter Healthcare Corporation | 16 |
| Mix2Vial Transfer Device | West Pharma. Services IL, Ltd. | 15 |
| Arisure | Yukon Medical, LLC | 13 |
| ViaLok | Yukon Medical, LLC | 12 |
| ICU Medical | ICU Medical, Inc | 12 |
| Codan | Codan US Corp. | 10 |
| SmartSite | Yukon Medical, LLC | 10 |
Showing 12 of 233. All products under Set, I.V. Fluid Transfer
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K231071 | 2024-01-19 |
| K232875 | 2023-12-14 |
| K230988 | 2023-12-01 |
| K230464 | 2023-05-22 |
| K213513 | 2022-08-31 |
Recalls
3 of these are Class I. Class I is the FDA’s most serious grade: a reasonable probability of serious injury or death. 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 |
|---|---|---|---|---|---|
| 2018-12-26 | Class I | Device Design | Adverse events have been reported with the use of oxytocin in conjunction with the 13mm Vial2Bag DC in pregnant women. Vial2Bag is recalled due to similarities with 13mm Vial2Bag DC. | 4.9 million units | 2022-07-20 |
| 2018-12-26 | Class I | Device Design | Adverse events have been reported with the use of oxytocin in conjunction with the product in pregnant women. There is a possibility that the device may cause inadequate admixing of drug with the solution in the IV bag. This could lead to | 3.9 million units | 2022-07-20 |
| 2018-12-26 | Class I | Device Design | Adverse events have been reported with the use of oxytocin in conjunction with the 13mm Vial2Bag DC in pregnant women. Vial2Bag DC 20mm is recalled due to similarities with 13mm Vial2Bag DC. | 30 million units | 2022-07-20 |
| 2017-10-06 | Class II | Process control | Medimop is recalling certain lots of this product Vial2Bag DC due to the potential of the IV Port separating from the Via12Bag DC body during the drug reconstitution I IV Set attachment process. | 453,600 units | 2024-01-23 |
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.