Qualified source record
TRANSLUMINAL
TRANSLUMINAL is listed in FDA device registration data in pompey Meurthe-et-Moselle, FR with the establishment role “Manufacture Medical Device for Another Party (Contract Manufacturer).” This qualified source record does not establish FDA approval, current capacity, or suitability for a project.
- Company type
- FDA-registered contract manufacturing establishment
- Source-reported role
- Manufacture Medical Device for Another Party (Contract Manufacturer)
- Source identifier
- 3022505496
- Owner/operator in source
- transluminal
- Company locations
- pompey Meurthe-et-Moselle, France
Locality and country come from the registered establishment record; the registered street address is not republished.
- Services & equipment
- Industries served
- Source checked
- 2026-09-07
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