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Medline

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline FDA UDI
Generic Name
Breathing circuit tube holder FDA UDI
Device Name
ANESTHESIA CIRCUIT TREE FDA UDI
Model / Reference
DYNJAATREE1 FDA UDI
Description
ANESTHESIA CIRCUIT TREE FDA UDI

Identifiers

Catalog Number
DYNJAATREE1 FDA UDI
Primary DI / UDI-DI
40080196150091 FDA UDI
FDA Product Code
JAY FDA UDI
GMDN Term
Breathing circuit tube holder FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5280 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Breathing circuit tube holder

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

Similar devices

Also classified as Breathing circuit tube holder.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI afb0a216-579c-4480-a4b2-98df8dd0b59c 35 fields · synced May 31, 2026