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spyhgmotensiophone, infant size velcro cuff pull through strap 1382

by Rudolf Riester GmbH & Co. KG

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 Number04045396001954 UDI-DI Date31 Aug 2016ListedStatusListed 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  • Withdrawn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
spyhgmotensiophone, infant size velcro cuff pull through strap
Generic Name
Aneroid manual sphygmomanometer
Model / Ref / Catalog
1382
Primary DI / UDI-DI
04045396001954
510(k) Number
FDA Product Code
DXN
GMDN Term
Aneroid manual sphygmomanometer
Device Class
Class II
Regulation Number
870.1130
GUDID distribution status
In Commercial Distribution

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Properties

  • Lot / Batch Number
  • Manufacturing Date

Other properties (12)

  • 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
  • Serial Number: No
  • Expiration Date: No