FDA UDI Not in Commercial Distribution 🇺🇸 United States

PlumePort

DI: 00815198012021 · Model: ActiV · Buffalo Filter
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
PlumePort
Primary DI
00815198012021
Version / Model
ActiV
Catalog Number
PP010CS
Company Name
Buffalo Filter
Labeler DUNS
787855907
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-01-05
Public Version
3
Public Version Date
2022-04-22
Public Version Status
Update
Public Device Record Key
641a39f8-0680-4cad-a9e6-6a69a6ea5240
Distribution End Date
2022-04-21

Device Description

Laparoscopic Plume Filtration Device

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
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
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
NKC Tubing/Tubing With Filter, Insufflation, Laparoscopic

GMDN Terms

Code Name
60836 Laparoscopic plume filter

Identifiers

Type ID
Package 10815198012028
Primary 00815198012021

Customer Contacts

Phone
716-835-7000