FDA UDI In Commercial Distribution 🇺🇸 United States

Suction Canister Kit

DI: 00810050862233 · Model: 099-0150 · LIFEPORT, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Suction Canister Kit
Primary DI
00810050862233
Version / Model
099-0150
Company Name
LIFEPORT, LLC
Labeler DUNS
556196210
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-10-17
Public Version
1
Public Version Date
2022-10-25
Public Version Status
New
Public Device Record Key
83b2490f-24ed-48cc-81b2-c7116d955250

Device Description

SUCTION CANISTER KIT, DISS, W/O BRACKET, W/LINER, W/ HANDLE

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
Yes
Has Serial Number
Yes
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
KDQ Bottle, Collection, Vacuum

GMDN Terms

Code Name
42446 Suction/irrigation system canister/bottle holder, single-use

Identifiers

Type ID
Primary 00810050862233

Customer Contacts

Phone
360-225-1212