Skip to content

CNAP® Monitor 500 V1.5

by CNSystems Medizintechnik GmbH 2 variants

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 Number09120073931436 UDI-DI Date25 May 2018ListedStatusListed 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  • Withdrawn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
CNAP® Monitor 500
Generic Name
Patient monitoring system module, blood pressure, noninvasive
Model / Ref / Catalog
V1.5, 21-FHCN-15536
Primary DI / UDI-DI
09120073931436
510(k) Number
FDA Product Code
DXN
GMDN Term
Patient monitoring system module, blood pressure, noninvasive
Device Class
Class II
Regulation Number
870.1130
GUDID distribution status
Not in Commercial Distribution
MRI Safety
MR Unsafe

Related devices

Cleared under the same submission (K082599)

Show all (12)

Other devices from CNSystems Medizintechnik GmbH

See all devices from CNSystems Medizintechnik GmbH →

Properties

  • Prescription Use
  • Serial Number
  • Manufacturing Date

Other properties (11)

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