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Emergency Medical Products

FDA UDI

Class II (US FDA UDI)

by Emergency Medical Products, Inc.

Identity

Trade Name
Emergency Medical Products FDA UDI
Generic Name
Blood pressure cuff, single-use FDA UDI
Device Name
Disposable Softcheck Cuff Assortment Pack FDA UDI
Model / Reference
172500C FDA UDI
Description
Disposable Softcheck Cuff Assortment Pack FDA UDI

Identifiers

Primary DI / UDI-DI
00851772007021 FDA UDI
FDA Product Code
DXQ FDA UDI
GMDN Term
Blood pressure cuff, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1120 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

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, single-use

Emergency Medical Products by Emergency Medical Products, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Blood pressure cuff, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b48b7a76-2060-4223-bee2-f36e62c393bf 33 fields · synced May 30, 2026