Precision Medical

FDA UDI

Class II (US FDA UDI)

by Precision Medical, Inc.

Identity

Trade Name: Precision Medical FDA UDI
Generic Name: General-purpose suction system, line-powered FDA UDI
Device Name: PM60,ASPIRATOR,EASY VAC,230V,50HZ FDA UDI
Model / Reference: PM60E FDA UDI
Description: PM60,ASPIRATOR,EASY VAC,230V,50HZ FDA UDI

Identifiers

Primary DI / UDI-DI: 00855887006634 FDA UDI
FDA Product Code: BTA FDA UDI
GMDN Term: General-purpose suction system, line-powered FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 878.4780 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

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: General-purpose suction system, line-powered

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

Similar devices

Also classified as General-purpose suction system, line-powered.

JETSTREAM — Bayer Healthcare · Class II
JETSTREAM™ PVCN100 — Boston Scientific · Class II
Winx® — Apnicure, Inc. · Class II
Meconium Aspirator — Neotech Products LLC · Class II
Snorkel — Neotech Products LLC · Class II
ANGIOJET — Bayer Healthcare · Class III
Winx® — Apnicure, Inc. · Class II
Winx® — Apnicure, Inc. · Class II

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: Precision Medical, Inc.

Sources (1)

FDA UDI 321878ac-efc1-4f06-ba31-61ffca885095 33 fields · synced May 30, 2026