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Rusch IPN041636

by Teleflex Incorporated

Ref 112682-000085

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 23 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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-04026704325306 Basic UDI-DI 04026704325306UDI-DIDate6 Jul 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04026704325306 UDI-DI Date16 Oct 2015ListedStatusListed 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 23 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  • Withdrawn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
Super Safety Silk Endotracheal Tube - with Cuff - Murphy - Sterile Pack EUDAMED
Rusch GUDID
Generic Name
Basic endotracheal tube, single-use
Device Name
Tracheal Tube, Cuffed, Murphy
Model / Ref / Catalog
112682-000085 EUDAMED
IPN041636 GUDID
112682085 GUDID
Primary DI / UDI-DI
04026704325306
Basic UDI-DI
B-04026704325306
510(k) Number
FDA Product Code
BTR
EMDN Code
R01030201 Endotracheal tubes, cuffed, not reinforced
GMDN Term
Basic endotracheal tube, single-use
Device Class
Class IIa EUDAMED
Class II GUDID
Regulation Number
868.5730
EU market of registration
Ireland
GUDID distribution status
In Commercial Distribution
Size
Height — 28 Millimeter
Width — 28 Millimeter
Outer Diameter — 12.4 Millimeter
Length — 345 Millimeter

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / ReferenceEUDAMED
112682-000085
GUDID
IPN041636
Device ClassEUDAMED
Class IIa
GUDID
Class II

Related devices

Category: Basic endotracheal tube, single-use

Cleared under the same submission (K132415)

Show all (12)

Other devices from Teleflex Incorporated

See all devices from Teleflex Incorporated →

Properties

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

Other properties (18)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: 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