F-27
Reprocessing Tracking Slip
دليل السياسات والإجراءات في التخدير — Section M

Form F-27 Preview

Reprocessing Tracking Slip (1-Page Table Format)

REPROCESSING TRACKING SLIP
(Airway Devices / Ultrasound Probes)
Hospital: ________________________ | Dept of Anesthesia / CSSD Form Code: F-27 | Version: ___ | Effective: ___ | PAGE 1 of 1
SECTION 1 — ITEM IDENTIFICATION
Date: ______/______/_________
Time: ___________________
Area:   OR    NORA    PACU    Block Area
Patient MRN/Case ID (optional per policy):
________________________________________________
Item category:    Airway device    Laryngoscope blade/handle    Bronchoscope    Ultrasound probe    Other: _________________

Item description/model:
________________________________________________
Asset/Serial number (if applicable):
________________________________________________
Contamination level:    Routine use    Visible soil/blood    Isolation case
Isolation Precautions:    Contact    Droplet    Airborne
SECTION 2 — REQUIRED REPROCESSING LEVEL
Low-level disinfection (LLD)       High-level disinfection (HLD)       Sterilization
IFU reference available:    Yes    No
Notes: _________________________________________________________________________________________________________
SECTION 3 — SENT TO CSSD / HLD
Placed in closed container/bag labeled:
Yes    No

Sent to:
CSSD Sterilization    HLD Unit    Other: ______________
Sent by (Name/Sign):
________________________________________________
Time: ________________

Received by CSSD/HLD (Name/Sign):
________________________________________________
Time: ________________
SECTION 4 — PROCESSING COMPLETION (CSSD/HLD)
Method used:
HLD    Sterilization    Other: ________________

Cycle/Batch # (if applicable):
________________________________________________
Processing date/time:
________________________________________________

Processed by (Name/Initials):
________________________________________________
SECTION 5 — RETURN TO CLINICAL AREA / STORAGE
Returned to area:    OR    NORA    PACU    Block Area
Time: ________________

Packaging integrity verified (if applicable):
Yes    No

Stored in clean designated storage:
Yes    No
Returned by CSSD/HLD (Name/Sign):

________________________________________________


Received by clinical area (Name/Sign):

________________________________________________
Traceability supports infection prevention audits and safe reuse of semi-critical/critical devices.