FDA UDI In Commercial Distribution 🇺🇸 United States

Manoscan

DI: 07290101363729 · Model: 800029 · Covidien LP
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Manoscan
Primary DI
07290101363729
Version / Model
800029
Company Name
Covidien LP
Labeler DUNS
058614483
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-03-24
Public Version
6
Public Version Date
2023-10-18
Public Version Status
Update
Public Device Record Key
2c712156-6c12-4809-9569-224b50cf5fc0

Device Description

Non SSI Cal Chamber Mount 3DAR

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
No
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
FFX SYSTEM, GASTROINTESTINAL MOTILITY (ELECTRICAL)

GMDN Terms

Code Name
35053 Manometric gastrointestinal motility analysis system

Identifiers

Type ID
Primary 07290101363729

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K151086 000