← Back to catalogue

Vital Signs™ Catheter Mount, Disposable With Flextube, (15mmF -22mmF), 150mm an…

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref M1040141

by AirLife Finland Oy

Identity

Trade Name
Vital Signs™ Catheter Mount, Disposable With Flextube, (15mmF -22mmF), 150mm and Double Swivel Elbow with Suction Port EUDAMED
Vital Signs™ FDA UDI
Generic Name
Breathing circuit catheter mount, single-use FDA UDI
Device Name
Vital Signs™ Mobile Catheter Mounts EUDAMED
Vital Signs™ Catheter Mount, Disposable With Flextube, (15mmF -22mmF), 150mm and Double Swivel Elbow with Suction Port FDA UDI
Model / Reference
M1040141 EUDAMEDFDA UDI
Description
Vital Signs™ Catheter Mount, Disposable With Flextube, (15mmF -22mmF), 150mm and Double Swivel Elbow with Suction Port FDA UDI

Identifiers

Catalog Number
M1040141 FDA UDI
Primary DI / UDI-DI
10889483602546 EUDAMEDFDA UDI
Basic UDI-DI
B-10889483602546 EUDAMED
FDA Product Code
BZA FDA UDI
EMDN Code
R020202 MOBILE CATHETER MOUNTS EUDAMED
GMDN Term
Breathing circuit catheter mount, single-use FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
868.5810 FDA UDI
Market of Registration
Finland EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

Vital Signs™ Catheter Mount, Disposable With Flextube, (15mmF -22mmF), 150mm an… by AirLife Finland Oy — Class IIa — MDD, FDA UDI — listed in EUDAMED, FDA GUDID

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

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

Manufacturer

Manufacturer
AirLife Finland Oy
EUDAMED SRN
FI-MF-000001482

Sources (2)

  • EUDAMED 4152772f-68b5-41e7-abf6-6e62dafa33fb 61 fields · synced Oct 10, 2026
  • FDA UDI ab072118-fe53-4a32-913a-01be149bebc4 35 fields · synced May 30, 2026