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Air-Q3 Self Pressurizing ILA with Automatic Cuff Inflation and GA Size 0.0

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 60005Model Air-Q®3 Supraglottic Airway Mask (SGA)

by SunMed

Identity

Trade Name
Air-Q3 Self Pressurizing ILA with Automatic Cuff Inflation and GA Size 0.0 EUDAMED
Air-Q3® FDA UDI
Generic Name
Laryngeal mask airway, single-use FDA UDI
Device Name
Air-Q3 Self Pressurizing ILA with Automatic Cuff Inflation and GA Size 0.0 FDA UDI
Model / Reference
Air-Q®3 Supraglottic Airway Mask (SGA) EUDAMED
60005 EUDAMEDFDA UDI
Description
Air-Q3 Self Pressurizing ILA with Automatic Cuff Inflation and GA Size 0.0 FDA UDI

Identifiers

Catalog Number
60005 FDA UDI
Primary DI / UDI-DI
10889483480526 EUDAMEDFDA UDI
Basic UDI-DI
0889483Air-Q3DF EUDAMED
FDA Product Code
CAE FDA UDI
EMDN Code
R01020199 LARYNGEAL MASKS - OTHER EUDAMED
GMDN Term
Laryngeal mask airway, single-use FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
868.5110 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

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 Safe FDA UDI

Air-Q3 Self Pressurizing ILA with Automatic Cuff Inflation and GA Size 0.0 by SunMed — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
SunMed
EUDAMED SRN
US-MF-000009164
Authorised Representative
Medical Technology Promedt Consulting GmbH DE-AR-000000085

Sources (2)

  • EUDAMED 1aee848d-6a09-4d9d-9899-22655cada5ed 61 fields · synced Jul 30, 2026
  • FDA UDI e80a2e9d-38a4-41d2-80ff-c1a3deb7e51d 36 fields · synced May 30, 2026