Pro's Combo™

FDA UDI

Class II (US FDA UDI)

by American Diagnostic Corporation

Identity

Trade Name: Pro's Combo™ FDA UDI
Generic Name: Aneroid manual sphygmomanometer FDA UDI
Device Name: Pro's Combo 778/606 Kit,Adult, Black, LF FDA UDI
Model / Reference: 778-606-11ABK FDA UDI
Description: Pro's Combo 778/606 Kit,Adult, Black, LF FDA UDI

Identifiers

Catalog Number: 778-606-11ABK FDA UDI
Primary DI / UDI-DI: 00634782094027 FDA UDI
FDA Product Code: DXQ FDA UDI
LDE FDA UDI
GMDN Term: Aneroid manual sphygmomanometer FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 870.1120 FDA UDI
870.1875 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Aneroid manual sphygmomanometer Mechanical external stethoscope

Pro's Combo™ by American Diagnostic Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: American Diagnostic Corporation

Sources (1)

FDA UDI b1f002ed-3603-4214-957f-a5d40fc212f1 37 fields · synced May 30, 2026