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Vital Signs™ Breathing Circuit, Expandable, Pediatric, Disposable, 1.8 m/72 in With Unifilter Junior, Gas Sampling Elbow, Vent Tube, 1.0 m and 1 L Bag

by AirLife Finland Oy

Ref M1132659

Active European Union. Also listed in GUDID (US).

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

None found

in data synced 25 Oct 2026

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-10889483603130 Basic UDI-DI 10889483603130UDI-DIDate13 Aug 2025RegisteredStatusActive
United StatesGUDID listing GUDID Number10889483603130 UDI-DI Date2 Apr 2025ListedStatusListed GUDID: in commercial distribution

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 25 Oct 2026.

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDD Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade Name
Vital Signs™ Breathing Circuit, Expandable, Pediatric, Disposable, 1.8 m/72 in With Unifilter Junior, Gas Sampling Elbow, Vent Tube, 1.0 m and 1 L Bag EUDAMED
Vital Signs™ GUDID
Generic Name
Anaesthesia breathing circuit, single-use
Device Name
Vital Signs™ Breathing Circuits, w/o Water Trap
Model / Ref / Catalog
M1132659
Primary DI / UDI-DI
10889483603130
Basic UDI-DI
B-10889483603130
510(k) Number
FDA Product Code
CAH
EMDN Code
R02010101 Breathing circuits, w/o water trap
GMDN Term
Anaesthesia breathing circuit, single-use
Device Class
Class IIa EUDAMED
Class II GUDID
Regulation Number
868.5260
EU market of registration
Finland
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device ClassEUDAMED
Class IIa
GUDID
Class II

Manufacturer details

EUDAMED SRN
FI-MF-000001482

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Properties

  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date

Other properties (18)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No