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Smoothline Green System Laryngoscope Blade, MAC 0

EUDAMEDFDA UDI

Class I (EU MDR)

Ref H9020

by PROACT Medical Ltd.

Identity

Trade Name
Smoothline Green System Laryngoscope Blade, MAC 0 EUDAMED
PROACT Smoothline FDA UDI
Generic Name
Laryngoscope blade, reusable FDA UDI
Device Name
Smoothline Green System Laryngoscope Blades EUDAMED
Smoothline Green System Laryngoscope Blade, MAC 0 FDA UDI
Model / Reference
H9020 EUDAMEDFDA UDI
Description
Smoothline Green System Laryngoscope Blade, MAC 0 FDA UDI

Identifiers

Catalog Number
H9020 FDA UDI
Primary DI / UDI-DI
25060179633750 EUDAMEDFDA UDI
Basic UDI-DI
50560945SMOOTHLINESATINNZ EUDAMED
Direct Marketing DI
15060179633753 EUDAMED
FDA Product Code
CCW FDA UDI
EMDN Code
Z12021003 LARYNGOSCOPES EUDAMED
GMDN Term
Laryngoscope blade, reusable FDA UDI

Classification

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

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

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Laryngoscope blade, reusable

Smoothline Green System Laryngoscope Blade, MAC 0 by PROACT Medical Ltd. — 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

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Manufacturer

Manufacturer
PROACT Medical Ltd.
EUDAMED SRN
GB-MF-000006294
Authorised Representative
Acorn Regulatory Consultancy Services Ltd IE-AR-000000592

Sources (2)

  • EUDAMED 918fe582-ee83-443b-af49-b4de84e69a1e 61 fields · synced Jul 31, 2026
  • FDA UDI 41554774-b308-4522-a9c1-dd9d04fa174d 36 fields · synced May 30, 2026