FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 00724995201777 · Model: Acu-sInQ Leak Test · Corporation Steris Canada
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
00724995201777
Version / Model
Acu-sInQ Leak Test
Catalog Number
600832OKN
Company Name
Corporation Steris Canada
Labeler DUNS
202659140
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-10-16
Public Version
4
Public Version Date
2021-08-09
Public Version Status
Update
Public Device Record Key
3dd219ad-fa22-4f5e-b174-51c75622e383

Device Description

The Olympus Leak Test Adapter used with the Acu-sinQ Complete Endoscope Cleaning Aid System.

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
FEB Accessories, cleaning, for endoscope

GMDN Terms

Code Name
38460 Invasive medical device leak tester, mechanical

Identifiers

Type ID
Primary 00724995201777
Previous 00724995167769

Customer Contacts