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E+r Ld-737

by Honsun (Nantong) Co., Ltd 2 variants

E+r Ld-737 is a Class II device made by Honsun (Nantong) Co., Ltd, cleared under FDA 510(k) K131463 on 8 Jul 2013 and listed in FDA GUDID since 27 Sep 2020 (UDI-DI 01697038425005), active as of 22 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

510(k) K131463

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number01697038425005 UDI-DI Date27 Sep 2020ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK131463 Date8 Jul 2013DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K131463 decided 8 Jul 2013 Active
  • FDA GUDID UDI-DI 01697038425005 listed 27 Sep 2020 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K131463
  2. Listed FDA GUDID 01697038425005

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
E+r
Generic name
Automatic-inflation electronic sphygmomanometer, portable, finger
Model / reference
LD-737
Primary DI / UDI-DI
01697038425005
510(k) Number
FDA product code
DXN
GMDN term
Automatic-inflation electronic sphygmomanometer, portable, finger
Device class
Class II
Regulation number
870.1130
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code DXN (System, Measurement, Blood-Pressure, Non-Invasive).

Other devices from Honsun (Nantong) Co., Ltd

See all devices from Honsun (Nantong) Co., Ltd →

Properties

  • Contains latex
  • Lot / batch number
  • Manufacturing date
Other properties (12, all answered No)