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Veridian

FDA UDI

Class II (US FDA UDI)

by Veridian Healthcare

Identity

Trade Name
VERIDIAN FDA UDI
Generic Name
Aneroid manual sphygmomanometer FDA UDI
Device Name
Self-Taking Home Blood Pressure Kit With Attached Stethoscope, Latex Free, Adult FDA UDI
Model / Reference
01-5501 FDA UDI
Description
Self-Taking Home Blood Pressure Kit With Attached Stethoscope, Latex Free, Adult FDA UDI

Identifiers

Primary DI / UDI-DI
00845717003223 FDA UDI
510(k) Number
K082542 FDA UDI
FDA Product Code
DXN FDA UDI
GMDN Term
Aneroid manual sphygmomanometer FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1130 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Aneroid manual sphygmomanometer

Veridian by Veridian Healthcare — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Aneroid manual sphygmomanometer.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Veridian Healthcare

Sources (1)

  • FDA UDI 8a8a48d3-c8f8-4472-94f4-64831aaeda49 35 fields · synced May 30, 2026