FDA UDI In Commercial Distribution 🇺🇸 United States

BEMIS

DI: 20073088150565 · Model: 8002 055 N · BEMIS MANUFACTURING COMPANY
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
BEMIS
Primary DI
20073088150565
Version / Model
8002 055 N
Catalog Number
8002 055 N
Company Name
BEMIS MANUFACTURING COMPANY
Labeler DUNS
006072078
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-10-15
Public Version
1
Public Version Date
2024-10-23
Public Version Status
New
Public Device Record Key
d4aeb287-ab34-4aef-9c4f-d8ad94b27c49

Device Description

800CC HIFLOW SOLO SUCTION CANISTER WITH AEROSTAT FILTER, FLOAT VALVE SHUTOFF WITH GREEN LID

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
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
KDQ Bottle, Collection, Vacuum

GMDN Terms

Code Name
34858 Surgical suction system collection container, single-use

Identifiers

Type ID
Primary 20073088150565

Device Sizes

Type Value Unit Text
Total Volume 800 Milliliter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
KEEP AWAY FROM SUNLIGHT