FDA UDI In Commercial Distribution 🇺🇸 United States

BEMIS

DI: 10073088149272 · Model: 175 020 · Bemis de México, S.A. de C.V.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
32

Basic Information

Brand Name
BEMIS
Primary DI
10073088149272
Version / Model
175 020
Catalog Number
175 020
Company Name
Bemis de México, S.A. de C.V.
Labeler DUNS
589153555
Distribution Status
In Commercial Distribution
Device Count in Pkg
32
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
6d015a93-c884-4324-874c-9bb15d9c01a7

Device Description

5 QUART 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

GMDN Terms

Code Name
35429 Sharps container

Identifiers

Type ID
Primary 10073088149272
Unit of Use 00073088149275

Premarket Submissions

Submission Number Supplement Number
K953797 000

Device Sizes

Type Value Unit Text
Total Volume 5 Quart