← Back to catalogue

Hemostasis Adapter

FDA UDI

Class II (US FDA UDI)

by Stereotaxis, Inc.

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

Similar devices

Also classified as Cardiac mapping system workstation.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Stereotaxis, Inc.

Sources (1)

  • FDA UDI 3d740963-7fcc-45b4-ab4b-9388c355907d 35 fields · synced May 30, 2026