← Back to catalogue

Hydra Conventional Laryngoscope Handle, Stubby

EUDAMEDFDA UDI

Class I (EU MDR)

Ref HYCVH003

by PROACT Medical Ltd.

Identity

Trade Name
Hydra Conventional Laryngoscope Handle, Stubby EUDAMED
PROACT Metal Max FDA UDI
Generic Name
Laryngoscope handle, reusable FDA UDI
Device Name
Hydra Conventional Laryngoscope Handles EUDAMED
Hydra Conventional Laryngoscope Handle, Stubby FDA UDI
Model / Reference
HYCVH003 EUDAMEDFDA UDI
Description
Hydra Conventional Laryngoscope Handle, Stubby FDA UDI

Identifiers

Catalog Number
HYCVH003 FDA UDI
Primary DI / UDI-DI
25056094500291 EUDAMEDFDA UDI
Basic UDI-DI
50560945HYCVHMN EUDAMED
Direct Marketing DI
15056094500294 EUDAMED
FDA Product Code
CCW FDA UDI
EMDN Code
Z12021003 LARYNGOSCOPES EUDAMED
GMDN Term
Laryngoscope handle, reusable FDA UDI

Classification

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

Hydra Conventional Laryngoscope Handle, Stubby 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

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

Manufacturer

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

Sources (2)

  • EUDAMED 253092a1-7806-41fe-a0ff-2958d49c1f03 61 fields · synced Jun 19, 2026
  • FDA UDI 61c2aaee-62fb-437b-873a-287a252c6029 36 fields · synced May 30, 2026