XE7XH

ICD-11 MMS 2026-01

Testing of device from same lot or batch retained by manufacturer

Description

The investigation employed relevant empirical testing of the device of the same lot or batch as that of the suspected device in the reported adverse event in order to support the identification of possible causes for the adverse event. Testing was performed using the device retained by the manufacturer (i.e. was not shipped). Relevant testing would typically be based on test methods used for evaluating safety and performance as described in the latest relevant standards.

Index terms

  • Testing of device from same lot or batch retained by manufacturer

Sibling codes

  • XE18W – Device discarded
  • XE1XT – Testing of model variant
  • XE2ZR – Testing of device from other lot batch retained by manufacturer
  • XE3TW – Insufficient information available
  • XE4KV – Analysis of production records
  • XE4S0 – Testing of device from same lot batch returned from user
  • XE4X1 – Testing of device from other lot or batch returned from user
  • XE53L – Device not accessible for testing
  • XE59M – Analysis of data provided by user or third party
  • XE5AN – Incomplete device returned
  • XE6FS – Testing of patient sample or reference material using manufacturer's device
  • XE6Q2 – Type of investigation not yet determined
  • XE7GK – Communication or interviews
  • XE89L – Testing of patient sample or reference material using competitor's device
  • XE8BM – Trend analysis
  • XE8FB – Device not manufactured by reporting manufacturer
  • XE8UH – Historical data analysis
  • XE8XV – Testing of raw or starting materials
  • XE970 – Device not returned
  • XE9HD – Testing of actual or suspected device
  • XE9MY – Testing of patient sample or reference material using reference method

Foundation entity

Testing of device from same lot or batch retained by manufacturer – http://id.who.int/icd/entity/269680842

Part of: X: Extension Codes