CTO Safety Standards & Documentation 2

Question 1

Which OSHA standard primarily governs bloodborne pathogen exposure in an orthotics fabrication lab?

Accepted Answer

29 CFR 1910.1030

Answer

OSHA 29 CFR 1910.1030 covers bloodborne pathogen standards applicable when technicians handle patient-contact materials.

Question 2

When documenting a device modification requested by a practitioner, what must always be recorded in the work order?

Accepted Answer

Practitioner's verbal authorization and date

Answer

Work orders must document the authorizing practitioner and date to maintain a clear chain of accountability.

Question 3

What is the correct action when a technician notices a crack in a load-bearing thermoplastic orthosis component during quality inspection?

Accepted Answer

Reject the device and document the defect

Answer

Structural defects in load-bearing components are a safety failure; the device must be rejected and the defect documented.

Question 4

Which labeling requirement must appear on every finished orthotic device delivered to a patient in the US?

Accepted Answer

Device name, lot/serial number, and manufacturer information

Answer

FDA and CMS guidelines require device identification labeling including manufacturer info and tracking numbers on delivered orthoses.

Question 5

A technician is grinding carbon fiber components. Which PPE is MOST critical beyond eye protection?

Accepted Answer

N95 or P100 respirator

Answer

Carbon fiber dust is a pulmonary hazard; respiratory protection rated for fine particulates is essential during grinding.

(CTO) Certified Orthotic Technician Practice Test