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Vital Signs™ Manual Ventilation Tube for ABS Bag Arm, Expandable, Disposable, 1…

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref M1154610

by AirLife Finland Oy

Identity

Trade Name
Vital Signs™ Manual Ventilation Tube for ABS Bag Arm, Expandable, Disposable, 1.8 m/72 in With ABS Bag Arm Connector EUDAMED
Vital Signs™ FDA UDI
Generic Name
Anaesthesia breathing circuit, single-use FDA UDI
Device Name
Vital Signs™ Respiratory Circuits Connection Pipes EUDAMED
Vital Signs™ Manual Ventilation Tube for ABS Bag Arm, Expandable, Disposable, 1.8 m/72 in With ABS Bag Arm Connector FDA UDI
Model / Reference
M1154610 EUDAMEDFDA UDI
Description
Vital Signs™ Manual Ventilation Tube for ABS Bag Arm, Expandable, Disposable, 1.8 m/72 in With ABS Bag Arm Connector FDA UDI

Identifiers

Catalog Number
M1154610 FDA UDI
Primary DI / UDI-DI
10889483603352 EUDAMEDFDA UDI
Basic UDI-DI
B-10889483603352 EUDAMED
FDA Product Code
BYX FDA UDI
EMDN Code
R020301 RESPIRATORY CIRCUITS CONNECTION PIPES EUDAMED
GMDN Term
Anaesthesia breathing circuit, single-use FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
868.5860 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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Vital Signs™ Manual Ventilation Tube for ABS Bag Arm, Expandable, Disposable, 1… 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 a0d91f8f-366d-46d3-ace4-1525ebbbe20b 61 fields · synced Jun 18, 2026
  • FDA UDI 7a1b04c4-05ec-4b8f-b1c1-a34eca1ba9f2 36 fields · synced May 30, 2026