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Siconus

FDA UDI

Class I (US FDA UDI)

by Camber Spine Technologies

Identity

Trade Name
Siconus FDA UDI
Generic Name
Orthopaedic implant calibration pin FDA UDI
Device Name
Ø2.4mm x 230mm Trocar Steinmann Pin FDA UDI
Model / Reference
SCL-130-101 FDA UDI
Description
Ø2.4mm x 230mm Trocar Steinmann Pin FDA UDI

Identifiers

Primary DI / UDI-DI
B030SCL1301010 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Orthopaedic implant calibration pin FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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

Yes

FDA UDI

Lot / Batch Number

No

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 implant calibration pin

Siconus by Camber Spine Technologies — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic implant calibration pin.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Camber Spine Technologies

Sources (1)

  • FDA UDI b89f78e1-e74c-4471-96d7-3d646abb17ee 34 fields · synced May 31, 2026