precisa® N Shock Proof, Sphygmomanometer with 1tub 1364-107

by Rudolf Riester GmbH & Co. KG

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

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

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number04045396211681 UDI-DI	Date28 Jan 2021Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: precisa® N Shock Proof, Sphygmomanometer with 1tub
Generic Name: Aneroid manual sphygmomanometer
Model / Ref / Catalog: 1364-107

Primary DI / UDI-DI: 04045396211681
FDA Product Code: DXQ
GMDN Term: Aneroid manual sphygmomanometer

Device Class: Class II
Regulation Number: 870.1120
GUDID distribution status: In Commercial Distribution

Other devices from Rudolf Riester GmbH & Co. KG

Stethoscope duplex® 2.0 white, 4210-02

Class I
Velcro cuff 1 tube, adults, 107.005

Class II
schiötz C tonometer, inclined scale, silver 5112

Class II
schiötz B tonometer, inclined scale, silver 5111

Class II
e-mega® white, disinfectable one-piece cuff, adult size 1-tube 1370-150

Class II
precisa® N aluminium, child size velcro cuff, (2 tubes) 1363-130

Class II

See all devices from Rudolf Riester GmbH & Co. KG →

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