FDA UDI In Commercial Distribution 🇺🇸 United States

Ascendo

DI: 00724995221614 · Model: 00712934 · US Endoscopy
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Ascendo
Primary DI
00724995221614
Version / Model
00712934
Catalog Number
00712934
Company Name
US Endoscopy
Labeler DUNS
627879687
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-07-11
Public Version
1
Public Version Date
2023-07-19
Public Version Status
New
Public Device Record Key
c6e3f3e3-5446-4396-b316-eec6f8f8581f

Device Description

Ascendo Submucosal Lifting Agent

Device Characteristics

Single Use
Yes
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
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
PLL Submucosal injection agent

GMDN Terms

Code Name
62217 Submucosal lift solution/gel

Identifiers

Type ID
Package 20724995221618
Package 10724995221611
Primary 00724995221614

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K220434 000