FDA UDI In Commercial Distribution 🇺🇸 United States

Attest™

DI: 50707387236477 · Model: 1296F · 3M COMPANY
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
25

Basic Information

Brand Name
Attest™
Primary DI
50707387236477
Version / Model
1296F
Catalog Number
1296F
Company Name
3M COMPANY
Labeler DUNS
830016148
Distribution Status
In Commercial Distribution
Device Count in Pkg
25
Record Status
Published
Publish Date
2016-09-24
Public Version
4
Public Version Date
2023-12-04
Public Version Status
Update
Public Device Record Key
e90c3ee3-e4a7-4d30-b95d-59414fbe4ab7

Device Description

1296F STM PACK 5CNT/CS 25PK/CS 1CS/CTN

Device Characteristics

Single Use
Yes
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
No
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
FRC Indicator, biological sterilization process

GMDN Terms

Code Name
13732 Biological sterilization indicator

Identifiers

Type ID
Primary 50707387236477
Unit of Use 00707387236458

Customer Contacts