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HolstOR PRO™

EUDAMEDFDA UDI

Class I (EU MDR)

Ref H-PRO-410

by The O R Company Pty Ltd

Identity

Trade Name
HolstOR PRO™ EUDAMED
HolstOR Pro FDA UDI
Generic Name
Electrosurgical handpiece/electrode holder, reusable FDA UDI
Device Name
Surgical Instrument Holder EUDAMEDFDA UDI
Model / Reference
H-PRO-410 EUDAMED
410mm FDA UDI
Description
Surgical Instrument Holder FDA UDI

Identifiers

Catalog Number
HPRO-410 FDA UDI
Primary DI / UDI-DI
09349967002919 EUDAMEDFDA UDI
Basic UDI-DI
93499670INSTHLDR45686TX EUDAMED
FDA Product Code
MDM FDA UDI
EMDN Code
V9012 NON-SPECIALIST SURGICAL INSTRUMENTS AND KITS, SINGLE-USE EUDAMED
GMDN Term
Electrosurgical handpiece/electrode holder, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
878.4800 FDA UDI
Market of Registration
Poland 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

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

No

FDA UDI

Dimensions & Sizes

Size
Length — 410 Millimeter FDA UDI

Category: Surgical retractor/retraction system blade, single-use

HolstOR PRO™ by The O R Company Pty Ltd — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical retractor/retraction system blade, single-use.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
AU-MF-000010179
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (2)

  • EUDAMED 09f7c749-fecf-45a8-8932-4fb4665bed07 61 fields · synced Jun 18, 2026
  • FDA UDI fce3ab62-e1e5-4519-bf5e-443b786f1a99 35 fields · synced May 29, 2026