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Viva Diagnostic ADIME913-20-EL50

by Tiger Supplies Inc

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 Number00840309445634 UDI-DI Date15 Jun 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  • Withdrawn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
Viva Diagnostic
Generic Name
Analytical non-scalp cutaneous electrode
Model / Reference
ADIME913-20-EL50
Primary DI / UDI-DI
00840309445634
510(k) Number
FDA Product Code
DRX
GMDN Term
Analytical non-scalp cutaneous electrode
Device Class
Class II
Regulation Number
870.2360
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K113485)

Show all (9)

Other devices from Tiger Supplies Inc

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Properties

  • Single Use
  • Lot / Batch Number
  • Manufacturing Date

Other properties (11)

  • Sterile: 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
  • Serial Number: No
  • Expiration Date: No