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A-PULSE CASPro® Central Aortic Systolic Pressure Monitoring Device(Professional) T7100 Series

by Healthstats International Pte Ltd

Listed FDA GUDID listing, not in commercial distribution

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number08885014410043 UDI-DI Date23 Sep 2016ListedStatusListed GUDID: not in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
A-PULSE CASPro® Central Aortic Systolic Pressure Monitoring Device(Professional)
Generic Name
Blood pressure ambulatory recorder
Model / Reference
T7100 Series
Primary DI / UDI-DI
08885014410043
510(k) Number
FDA Product Code
DXN
GMDN Term
Blood pressure ambulatory recorder
Device Class
Class II
Regulation Number
870.1130
GUDID distribution status
Not in Commercial Distribution

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Properties

  • Serial Number

Other properties (13)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Lot / Batch Number: No
  • Expiration Date: No
  • Manufacturing Date: No