Identity
- Trade Name
- FLOWMATE® FDA UDI
- Generic Name
- Atherectomy system saline/lubricant pump FDA UDI
- Device Name
- FLOWMATE® Injector FDA UDI
- Model / Reference
- INJ100 FDA UDI
- Description
- FLOWMATE® Injector FDA UDI
Identifiers
- Catalog Number
- INJ100 FDA UDI
- Primary DI / UDI-DI
- 00801741067686 FDA UDI
- 510(k) Number
- K090621 FDA UDI
- FDA Product Code
- DXT FDA UDI
- GMDN Term
- Atherectomy system saline/lubricant pump FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.1650 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Atherectomy system saline/lubricant pump
Flowmate® by Bard Peripheral Vascular — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Atherectomy system saline/lubricant pump.
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Bard Peripheral Vascular
Sources (1)
- FDA UDI ae494685-05cf-42ac-a1c5-15df21356a50 36 fields · synced Jun 6, 2026