Identity
- Trade Name
- Vision FDA UDI
- Generic Name
- Surgical instrument washer/disinfector (chemical/thermal) FDA UDI
- Device Name
- The Vision Multi-Chamber Washer Disinfector is intended for use in the cleaning and intermediate level disinfection of soiled reusable utensils, trays, glassware, bedpans and urinals, rubber and plastic goods, simple hard-surfaced rigid surgical instruments (such as forceps and clamps) and other related articles found in healthcare facilities. FDA UDI
- Model / Reference
- Multi-Chamber FDA UDI
- Description
- The Vision Multi-Chamber Washer Disinfector is intended for use in the cleaning and intermediate level disinfection of soiled reusable utensils, trays, glassware, bedpans and urinals, rubber and plastic goods, simple hard-surfaced rigid surgical instruments (such as forceps and clamps) and other related articles found in healthcare facilities. FDA UDI
Identifiers
- Catalog Number
- FH81072 FDA UDI
- Primary DI / UDI-DI
- 00724995193133 FDA UDI
- FDA Product Code
- MEC FDA UDI
- GMDN Term
- Surgical instrument washer/disinfector (chemical/thermal) FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.6992 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
No
FDA UDI
Over-the-Counter
Yes
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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Surgical instrument washer/disinfector (chemical/thermal)
Vision by Corporation Steris Canada — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Corporation Steris Canada
Sources (1)
- FDA UDI 27b2b25b-a332-4ac9-bce3-ea42df371b7f 35 fields · synced Jun 8, 2026