Pro's Combo™

FDA UDI

Class I (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 768/603 Kit,Adult, Black, LF, 353BK, 321ST FDA UDI
Model / Reference: 768-603-11ASTKIT FDA UDI
Description: Pro's Combo 768/603 Kit,Adult, Black, LF, 353BK, 321ST FDA UDI

Identifiers

Catalog Number: 768-603-11ASTKIT FDA UDI
Primary DI / UDI-DI: 00634782099510 FDA UDI
FDA Product Code: LDE FDA UDI
DXQ FDA UDI
KYT FDA UDI
GMDN Term: Aneroid manual sphygmomanometer FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 870.1875 FDA UDI
870.1120 FDA UDI
880.6350 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 I — 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 I	Pending data

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Manufacturer

Manufacturer: American Diagnostic Corporation

Sources (1)

FDA UDI d82b3359-abd4-4548-b966-93a5a970d750 37 fields · synced May 30, 2026