← Back to catalogue

inspired™

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref 2096534-103

by Vincent Medical Manufacturing Co., Limited

Identity

Trade Name
inspired™ EUDAMEDFDA UDI
Generic Name
Inspiratory/expiratory limb respiratory tubing, reusable FDA UDI
Device Name
PATIENT TUBE,PEDIATRIC,REUSABLE,SILICONE,1.5m FDA UDI
Model / Reference
2096534-103 EUDAMEDFDA UDI
Description
PATIENT TUBE,PEDIATRIC,REUSABLE,SILICONE,1.5m FDA UDI

Identifiers

Primary DI / UDI-DI
14896138001018 EUDAMEDFDA UDI
Basic UDI-DI
B-14896138001018 EUDAMED
FDA Product Code
CAI FDA UDI
EMDN Code
R020199 BREATHING CIRCUITS AND KITS - OTHER EUDAMED
GMDN Term
Inspiratory/expiratory limb respiratory tubing, reusable FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
868.5240 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

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

Category: Inspiratory/expiratory limb respiratory tubing, reusable

inspired™ by Vincent Medical Manufacturing Co., Limited — Class I — MDD, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Inspiratory/expiratory limb respiratory tubing, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDD

United States Pending data

FDA UDI

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

Manufacturer

Sources (2)

  • FDA UDI 07071206-3655-448c-9d79-721c3df6339f 33 fields · synced Oct 5, 2026
  • EUDAMED e2ec9bf3-5365-44be-8de4-9c8352e93ac4 61 fields · synced Oct 5, 2026