Banclar Pg-800B19L

by Banclar Corp.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

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

Region	Authorization	Number	Date	Status
United States	GUDID listing	NumberG467101112BC0 UDI-DI	Date28 Apr 2023Listed	StatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: Banclar
Generic Name: Automatic-inflation electronic sphygmomanometer, portable, arm/wrist
Model / Reference: PG-800B19L

Primary DI / UDI-DI: G467101112BC0
510(k) Number: K200716
FDA Product Code: DXN
GMDN Term: Automatic-inflation electronic sphygmomanometer, portable, arm/wrist

Device Class: Class II
Regulation Number: 870.1130
GUDID distribution status: In Commercial Distribution

MRI Safety: MR Unsafe

Properties

Lot / Batch Number
Expiration 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
Manufacturing Date: No