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DORO® Halo Half Ring Radiolucent

FDA UDI

Class II (US FDA UDI)

by pro med instruments GmbH, Herstellung und Vertrieb medizinisch technischer Ausrüstung

Identity

Trade Name
DORO® Halo Half Ring Radiolucent FDA UDI
Generic Name
Surgical retraction system, reusable FDA UDI
Device Name
DORO® Halo Half Ring Radiolucent FDA UDI
Model / Reference
3037-03 FDA UDI
Description
DORO® Halo Half Ring Radiolucent FDA UDI

Identifiers

Primary DI / UDI-DI
04250435502402 FDA UDI
510(k) Number
K063494 FDA UDI
FDA Product Code
HBL FDA UDI
GMDN Term
Surgical retraction system, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4460 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical retraction system, reusable

DORO® Halo Half Ring Radiolucent by pro med instruments GmbH, Herstellung und Vertrieb medizinisch technischer Ausrüstung — Class II — FDA UDI — listed in FDA…

Similar devices

Also classified as Surgical retraction system, reusable.

Cleared under the same submission

K063494 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 902aa40a-2d1c-4fa7-b787-ea32837866e4 34 fields · synced Jun 8, 2026