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Adapter, Tube, Sample Pack

FDA UDI

Class I (US FDA UDI)

by A-M Systems, Inc.

Identity

Trade Name
Adapter, Tube, Sample Pack FDA UDI
Generic Name
Breathing mouthpiece, reusable FDA UDI
Device Name
Adapter, Tube, Sample Pack, 1134, 1135, 1136, 1138 FDA UDI
Model / Reference
Adapter, Tube, Sample Pack - 113300 FDA UDI
Description
Adapter, Tube, Sample Pack, 1134, 1135, 1136, 1138 FDA UDI

Identifiers

Catalog Number
113300 FDA UDI
Primary DI / UDI-DI
00817081027686 FDA UDI
FDA Product Code
BYP FDA UDI
GMDN Term
Breathing mouthpiece, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5620 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Breathing mouthpiece, reusable

Adapter, Tube, Sample Pack by A-M Systems, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Breathing mouthpiece, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
A-M Systems, Inc.

Sources (1)

  • FDA UDI ad117574-bb9b-469b-b529-b4c854efe2e6 35 fields · synced Jun 1, 2026