Data / Medical devices / China / Becton Dickinson Medical Devices Co., Ltd. Suzhou
Becton Dickinson Medical Devices Co., Ltd. Suzhou: FDA-registered device maker in Suzhou Jiangsu, China, 1 510(k) clearance
Becton Dickinson Medical Devices Co., Ltd. Suzhou is registered with the FDA (registration 3002601200) in Suzhou Jiangsu, China. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated May 31, 2022. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3002601200
- Address
- No. 5 Baiyu Road Suzhou Industrial Park, Suzhou Jiangsu, China, 215021
- Owner or operator
- Becton Dickinson and Company (9922032)
- Roles
- Contract manufacturer, Contract sterilizer, Manufacturer
- First device listed
- January 12, 2016
- Registered through
- 2026
- Brand names listed
- BD Angiocath IV Catheter, BD Saf-T-Intima Safety System, BD Saf-T-Intima Subcutaneous Catheter System, Liverty TIPS Access Set
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days | FOZ | 2 | Contract manufacturer, Contract sterilizer | accessdata.fda.gov |
| Introducer, Catheter | DYB | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| May 31, 2022 | K221440 | Liverty TIPS Access Set | DYB | Substantially Equivalent | Bard Peripheral Vascular, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Introducer, Catheter
- All makers of Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
Updated May 31, 2022. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.