← Back to catalogue

Airtraq SP Paediatric

EUDAMEDFDA UDI

Class I (EU MDR)

Ref A-031

by Prodol Medited Limited

Identity

Trade Name
Airtraq SP Paediatric EUDAMED
Airtraq FDA UDI
Generic Name
Channelled video intubation laryngoscope FDA UDI
Device Name
Airtraq Video Laryngoscopes and accesories. EUDAMED
Airtraq SP Pediatric FDA UDI
Model / Reference
A-031 EUDAMEDFDA UDI
Description
Airtraq SP Pediatric FDA UDI

Identifiers

Primary DI / UDI-DI
08436031030310 EUDAMEDFDA UDI
Basic UDI-DI
843603103PRODOLMEDKT EUDAMED
FDA Product Code
CCW FDA UDI
EMDN Code
Z12021003 LARYNGOSCOPES EUDAMED
GMDN Term
Channelled video intubation laryngoscope FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
868.5540 FDA UDI
Market of Registration
Spain 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

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

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
MRI Safety
MR Conditional FDA UDI

Category: Laryngoscope blade, reusable

Airtraq SP Paediatric by Prodol Medited Limited — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Laryngoscope blade, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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

Manufacturer

EUDAMED SRN
CN-MF-000014746
Authorised Representative
Prodol Meditec S.A. ES-AR-000005064

Sources (2)

  • EUDAMED 9aee3074-df0f-493d-936f-852df2341ad1 61 fields · synced Jul 15, 2026
  • FDA UDI de5ccdf8-811f-45e9-ae11-352572ce2c2b 33 fields · synced May 29, 2026