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Radius Plate PROlock II

FDA UDI

Class II (US FDA UDI)

by I.T.S. GmbH

Identity

Trade Name
Radius Plate PROlock II FDA UDI
Generic Name
Orthopaedic fixation plate, non-bioabsorbable FDA UDI
Device Name
Radius Plate PROlock II, Wide, 3-Hole, Right FDA UDI
Model / Reference
21033-3 FDA UDI
Description
Radius Plate PROlock II, Wide, 3-Hole, Right FDA UDI

Identifiers

Catalog Number
21033-3 FDA UDI
Primary DI / UDI-DI
09120047296905 FDA UDI
510(k) Number
K033756 FDA UDI
FDA Product Code
HRS FDA UDI
GMDN Term
Orthopaedic fixation plate, non-bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3030 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic fixation plate, non-bioabsorbable

Radius Plate PROlock II by I.T.S. GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic fixation plate, non-bioabsorbable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
I.T.S. GmbH

Sources (1)

  • FDA UDI 3c55ddf3-2fdd-49b3-80ed-91c4ffc73996 35 fields · synced Jun 8, 2026