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A-dec

FDA UDI

Class I (US FDA UDI)

by A-Dec, Inc.

Identity

Trade Name
A-dec FDA UDI
Generic Name
Medical device air compressor FDA UDI
Device Name
Smart-Vac 10 Dry Vacuum System FDA UDI
Model / Reference
DV10 FDA UDI
Description
Smart-Vac 10 Dry Vacuum System FDA UDI

Identifiers

Catalog Number
DV10 FDA UDI
Primary DI / UDI-DI
10194665003104 FDA UDI
FDA Product Code
NRD FDA UDI
GMDN Term
Medical device air compressor FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6640 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

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Medical device air compressor

A-dec by A-Dec, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medical device air compressor.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
A-Dec, Inc.

Sources (1)

  • FDA UDI ecb6b8f6-6e3a-4178-8292-d25ba64c2006 34 fields · synced May 31, 2026