← Back to catalogue

Expression MR LoFlo Sample Line, Airway Adapt., Adult

FDA UDI

Class II (US FDA UDI)

by Philips DS North America LLC

Identity

Trade Name
Expression MR LoFlo Sample Line, Airway Adapt., Adult FDA UDI
Generic Name
Breathing circuit catheter mount, single-use FDA UDI
Model / Reference
LoFlo Line, Adu Airway Adpt, Box 20 FDA UDI

Identifiers

Catalog Number
989803183291 FDA UDI
Primary DI / UDI-DI
10884838037837 FDA UDI
FDA Product Code
CCK FDA UDI
GMDN Term
Breathing circuit catheter mount, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.1400 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Breathing circuit catheter mount, single-use

Expression MR LoFlo Sample Line, Airway Adapt., Adult by Philips DS North America LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Breathing circuit catheter mount, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Philips DS North America LLC

Sources (1)

  • FDA UDI 07da1704-e65c-4790-af94-8fd24cb20faf 34 fields · synced Jun 8, 2026