FDA UDI In Commercial Distribution 🇺🇸 United States

Versaport

DI: 20884521081359 · Model: 179101 · Covidien LP
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Versaport
Primary DI
20884521081359
Version / Model
179101
Company Name
Covidien LP
Labeler DUNS
058614483
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-29
Public Version
7
Public Version Date
2023-10-13
Public Version Status
Update
Public Device Record Key
ef3c316c-69bc-4b97-9f1b-188e6b74e836

Device Description

V2 Bladed RT Obturator

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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GCJ Laparoscope, general & plastic surgery

GMDN Terms

Code Name
38456 Laparoscopic multi-instrument access port, single-use

Identifiers

Type ID
Package 10884521081352
Primary 20884521081359

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K963115 000

Device Sizes

Type Value Unit Text
Outer Diameter 5 Millimeter

Storage Conditions

Type
Handling Environment Temperature
Temperature Range
– 130 Degrees Fahrenheit