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Large Cuff, Bladder for Hem-907

FDA UDI

Class II (US FDA UDI)

by Omron Healthcare, Inc.

Identity

Trade Name
Large Cuff, Bladder for Hem-907 FDA UDI
Generic Name
Blood pressure cuff, reusable FDA UDI
Device Name
Blood Pressure Cuff for HEM-907 - Large FDA UDI
Model / Reference
HEM-907-CL19 FDA UDI
Description
Blood Pressure Cuff for HEM-907 - Large FDA UDI

Identifiers

Catalog Number
HEM-907-CL19 FDA UDI
Primary DI / UDI-DI
00073796907037 FDA UDI
510(k) Number
K032305 FDA UDI
FDA Product Code
DXN FDA UDI
GMDN Term
Blood pressure cuff, reusable 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

Yes

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: Blood pressure cuff, reusable

Large Cuff, Bladder for Hem-907 by Omron Healthcare, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Blood pressure cuff, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4b18fc65-02d3-45fb-bf78-490beaf9f4f7 36 fields · synced May 30, 2026