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Double Airline Tubing

FDA UDI

Class II (US FDA UDI)

by Millennium Medical Technologies, Inc.

Identity

Trade Name
Double Airline Tubing FDA UDI
Generic Name
Suction/irrigation tubing, single-use FDA UDI
Model / Reference
MAS-10002 FDA UDI

Identifiers

Primary DI / UDI-DI
00850000712393 FDA UDI
510(k) Number
K081039 FDA UDI
FDA Product Code
QPB FDA UDI
GMDN Term
Suction/irrigation tubing, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.5040 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Suction/irrigation tubing, single-use

Double Airline Tubing by Millennium Medical Technologies, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Suction/irrigation tubing, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e05b4d47-93bf-477b-8894-786f6365a065 33 fields · synced Jun 8, 2026