FDA UDI In Commercial Distribution 🇺🇸 United States

BEMIS

DI: 10073088149494 · Model: 3002 055 · BEMIS MANUFACTURING COMPANY
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
36

Basic Information

Brand Name
BEMIS
Primary DI
10073088149494
Version / Model
3002 055
Catalog Number
3002 055
Company Name
BEMIS MANUFACTURING COMPANY
Labeler DUNS
006072078
Distribution Status
In Commercial Distribution
Device Count in Pkg
36
Record Status
Published
Publish Date
2016-09-24
Public Version
7
Public Version Date
2022-11-28
Public Version Status
Update
Public Device Record Key
ef95a68b-3fa6-4fcd-9bf6-b76d52dcaa74

Device Description

3000CC HIFLOW SUCTION CANISTER WITH AEROSTAT FILTER, FLOAT VALVE SHUT OFF 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 10073088149494
Unit of Use 00073088149497

Device Sizes

Type Value Unit Text
Total Volume 3000 Milliliter

Storage Conditions

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