FDA UDI In Commercial Distribution 🇺🇸 United States

ManoScan

DI: 07290101364009 · Model: 800024 · Covidien LP
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ManoScan
Primary DI
07290101364009
Version / Model
800024
Company Name
Covidien LP
Labeler DUNS
058614483
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-12-05
Public Version
2
Public Version Date
2021-11-17
Public Version Status
Update
Public Device Record Key
54421298-ac1a-462c-97d5-4866a51e890b

Device Description

ManoScan AR Software

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
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
NEZ SYSTEM, IMAGING, GASTROINTESTINAL, WIRELESS, CAPSULE

GMDN Terms

Code Name
35053 Manometric gastrointestinal motility analysis system

Identifiers

Type ID
Primary 07290101364009

Customer Contacts