FDA UDI In Commercial Distribution 🇺🇸 United States

RapidVac

DI: 20884524000883 · Model: SEA3715 · Covidien LP
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
RapidVac
Primary DI
20884524000883
Version / Model
SEA3715
Company Name
Covidien LP
Labeler DUNS
058614483
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
7
Public Version Date
2023-03-16
Public Version Status
Update
Public Device Record Key
b6040b82-e47a-4bff-a870-8fb8dbb31db9

Device Description

Smoke Sponge Guard Tubing

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
FYD APPARATUS, EXHAUST, SURGICAL

GMDN Terms

Code Name
46483 Surgical plume evacuation system tube

Identifiers

Type ID
Package 10884524000886
Primary 20884524000883

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K980915 000

Device Sizes

Type Value Unit Text
Length 10 Feet
Outer Diameter 0.875 Inch

Storage Conditions

Type
Handling Environment Temperature
Temperature Range
-29 – 149 Degrees Fahrenheit
Type
Handling Environment Humidity
Temperature Range
0 – 75 Percent (%) Relative Humidity