FDA UDI In Commercial Distribution 🇺🇸 United States

V-PRO

DI: 00724995152673 · Model: max 2 · Steris Mexico, S. de R.L. de C.V.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
V-PRO
Primary DI
00724995152673
Version / Model
max 2
Catalog Number
VP50001101
Company Name
Steris Mexico, S. de R.L. de C.V.
Labeler DUNS
813116209
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-08-23
Public Version
6
Public Version Date
2024-02-27
Public Version Status
Update
Public Device Record Key
0f71cdf8-290d-413c-b423-70f679264e4e

Device Description

The V-PRO maX 2 Low Temperature Sterilization System is used in the terminal sterilization of properly prepared, cleaned, rinsed and dried medical devices utilizing VAPROX HC Sterilant.

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
MLR Sterilizer, chemical

GMDN Terms

Code Name
40567 Hydrogen peroxide gas sterilizer

Identifiers

Type ID
Primary 00724995152673

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K172754 000
K190103 000
K222093 000
K222543 000
K233065 000