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LoFlo Sidestream Consumables

FDA UDI

Class III (US FDA UDI)

by Zoll Medical Corporation

Identity

Trade Name
LoFlo Sidestream Consumables FDA UDI
Generic Name
Gas dehumidification tubing set, single-use FDA UDI
Device Name
KIT, ADAPTER, AIRWAY, ADULT/PEDIATRIC, BOX OF 10, (REF: 3572ADU-00) FDA UDI
Model / Reference
9355-0276 FDA UDI
Description
KIT, ADAPTER, AIRWAY, ADULT/PEDIATRIC, BOX OF 10, (REF: 3572ADU-00) FDA UDI

Identifiers

Primary DI / UDI-DI
00847946024000 FDA UDI
FDA Product Code
MKJ FDA UDI
GMDN Term
Gas dehumidification tubing set, single-use FDA UDI

Classification

Device Class
Class III FDA UDI
Regulation Number
870.5310 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Gas dehumidification tubing set, single-use

LoFlo Sidestream Consumables by Zoll Medical Corporation — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Gas dehumidification tubing set, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Zoll Medical Corporation

Sources (1)

  • FDA UDI 05dcaa7b-a44f-4223-bd46-0ccee77965ab 34 fields · synced Jun 8, 2026