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Zeitels Suspension Gallows

EUDAMEDFDA UDI

Class I (EU MDR)

Ref ZVG-100A

by Endocraft LLC

Identity

Trade Name
Endocraft LLC FDA UDI
Generic Name
Rigid laryngoscope positioner FDA UDI
Device Name
Zeitels Suspension Gallows EUDAMED
Zeitels Suspension Gallows positions and holds the laryngoscope and patient in ideal posture for surgery. This suspension mounts to the surgical bed, rather than on the patient's chest. FDA UDI
Model / Reference
ZVG-100A EUDAMED
ZVG100A FDA UDI
Description
Zeitels Suspension Gallows positions and holds the laryngoscope and patient in ideal posture for surgery. This suspension mounts to the surgical bed, rather than on the patient's chest. FDA UDI

Identifiers

Catalog Number
ZVG100A FDA UDI
Primary DI / UDI-DI
00860009975132 EUDAMEDFDA UDI
Basic UDI-DI
08600099751ZVG1007C EUDAMED
FDA Product Code
CCW FDA UDI
EMDN Code
Z12021003 LARYNGOSCOPES EUDAMED
GMDN Term
Rigid laryngoscope positioner FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
868.5540 FDA UDI
Market of Registration
Belgium EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Laryngoscope blade, reusable

Zeitels Suspension Gallows by Endocraft LLC — 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
Endocraft LLC
EUDAMED SRN
US-MF-000020169
Authorised Representative
MediMark Europe Sarl. FR-AR-000000182

Sources (2)

  • EUDAMED 5d71e464-506f-4e3b-b533-cfa9f9b3bcfe 61 fields · synced Jun 19, 2026
  • FDA UDI 916d43d4-8f9d-44f9-8b7c-4afa28b9c74e 35 fields · synced May 27, 2026