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SCHILLER ECG BWDSC C 1.1/0.75 x10 AHA DP

by Schiller Corp.

Listed FDA GUDID listing, no authorization on record

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 Number07613365003970 UDI-DI Date16 Sep 2026ListedStatusListed GUDID: 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  • Withdrawn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
Schiller
Generic Name
Electrocardiographic ambulatory recorder
Model / Ref / Catalog
ECG BWDSC C 1.1/0.75 x10 AHA DP, 2.400188
Primary DI / UDI-DI
07613365003970
510(k) Number
FDA Product Code
MWJ
GMDN Term
Electrocardiographic ambulatory recorder
Device Class
Class II
Regulation Number
870.2800
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Unsafe

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Properties

  • Prescription Use
  • Lot / Batch 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
  • Serial Number: No
  • Expiration Date: No