FDA UDI In Commercial Distribution 🇺🇸 United States

BEMIS

DI: 10073088151039 · Model: 102 020 · BEMIS MANUFACTURING COMPANY
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
30

Basic Information

Brand Name
BEMIS
Primary DI
10073088151039
Version / Model
102 020
Catalog Number
102 020
Company Name
BEMIS MANUFACTURING COMPANY
Labeler DUNS
006072078
Distribution Status
In Commercial Distribution
Device Count in Pkg
30
Record Status
Published
Publish Date
2016-09-24
Public Version
5
Public Version Date
2023-08-18
Public Version Status
Update
Public Device Record Key
4c32aa37-d144-4042-97a4-5a04fadea085

Device Description

2 GALLON BEIGE SHARPS CONTAINER

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
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
MMK Container, Sharps
FMI Needle, Hypodermic, Single Lumen

GMDN Terms

Code Name
35429 Sharps container

Identifiers

Type ID
Primary 10073088151039
Unit of Use 00073088151032

Premarket Submissions

Submission Number Supplement Number
K965248 000

Device Sizes

Type Value Unit Text
Total Volume 2 Gallon