FDA UDI In Commercial Distribution 🇺🇸 United States

ManoScan

DI: 04260167482248 · Model: MSS-3599 · Covidien LP
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Basic Information

Brand Name
ManoScan
Primary DI
04260167482248
Version / Model
MSS-3599
Company Name
Covidien LP
Labeler DUNS
058614483
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2017-07-05
Public Version
7
Public Version Date
2023-10-18
Public Version Status
Update
Public Device Record Key
61f94b37-73d5-4852-ac22-e62c53396dbc

Device Description

Assy, Retail Box of 10, ManoShield AR

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
No
Has Expiration Date
Yes
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 04260167482248
Unit of Use 10884521742734

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K151086 000