precisa® N plastic/metal manometer, double tube, without cuff 1361-100

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	Number04045396111349 UDI-DI	Date30 Aug 2016Listed	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Withdrawn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 plastic/metal manometer, double tube, without cuff
Generic Name: Aneroid manual sphygmomanometer
Model / Ref / Catalog: 1361-100

Primary DI / UDI-DI: 04045396111349
FDA Product Code: DXQ
GMDN Term: Aneroid manual sphygmomanometer

Device Class: Class II
Regulation Number: 870.1120
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