Identity
- Trade Name
- Hemostasis Adapter FDA UDI
- Generic Name
- Cardiac mapping system workstation FDA UDI
- Device Name
- Hemostasis Adapter IV Spares, Box, Device Count(5) FDA UDI
- Model / Reference
- IV-1 FDA UDI
- Description
- Hemostasis Adapter IV Spares, Box, Device Count(5) FDA UDI
Identifiers
- Catalog Number
- 0010011141 FDA UDI
- Primary DI / UDI-DI
- M58800100111411 FDA UDI
- 510(k) Number
- K071029 FDA UDI
- FDA Product Code
- DQX FDA UDI
- GMDN Term
- Cardiac mapping system workstation FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.1330 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Cardiac mapping system workstation
Hemostasis Adapter by Stereotaxis, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
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
- Stereotaxis, Inc.
Sources (1)
- FDA UDI 3d740963-7fcc-45b4-ab4b-9388c355907d 35 fields · synced May 30, 2026