FDA UDI Not in Commercial Distribution 🇺🇸 United States

VIA

DI: 00724995182014 · Model: 00717112 · US Endoscopy
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

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Basic Information

Brand Name
VIA
Primary DI
00724995182014
Version / Model
00717112
Catalog Number
00717112
Company Name
US Endoscopy
Labeler DUNS
627879687
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-02-06
Public Version
3
Public Version Date
2022-06-06
Public Version Status
Update
Public Device Record Key
ff0be996-ecb9-4d6c-b6a9-b3b413746e1e
Distribution End Date
2022-06-03

Device Description

The VIA procedure kit-custom includes transport pad, chux pad, basin, suction tubing, BioShield biopsy valve, biohazard sticker, lubricating jelly, enzymatic sponge and gowns.

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
NWU Endoscope introducer kit

GMDN Terms

Code Name
61950 Endoscopy preparation kit

Identifiers

Type ID
Previous 00816765014943
Package 10724995182011
Primary 00724995182014

Customer Contacts