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Aseptico

FDA UDI

Class I (US FDA UDI)

by Aseptico, Inc.

Identity

Trade Name
Aseptico FDA UDI
Generic Name
Dental delivery system FDA UDI
Device Name
Express Air 2 Portable Dental System FDA UDI
Model / Reference
ADU-17A2 FDA UDI
Description
Express Air 2 Portable Dental System FDA UDI

Identifiers

Primary DI / UDI-DI
10817417021576 FDA UDI
510(k) Number
K905401 FDA UDI
FDA Product Code
EIA FDA UDI
GMDN Term
Dental delivery system 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

Yes

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental delivery system

Aseptico by Aseptico, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental delivery system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Aseptico, Inc.

Sources (1)

  • FDA UDI 632804d3-6ca2-4e23-b508-c85aa30e3207 36 fields · synced May 30, 2026