FDA UDI In Commercial Distribution 🇺🇸 United States

Aura™

DI: 00051131499966 · Model: 1870+ · 3M Company
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
20

Basic Information

Brand Name
Aura™
Primary DI
00051131499966
Version / Model
1870+
Catalog Number
1870+
Company Name
3M Company
Labeler DUNS
080644849
Distribution Status
In Commercial Distribution
Device Count in Pkg
20
Record Status
Published
Publish Date
2016-08-03
Public Version
8
Public Version Date
2023-12-22
Public Version Status
Update
Public Device Record Key
2ee7519c-a856-482a-ac36-ef19419430ab

Device Description

1870+ HEALTH CARE PART RESP. 120/CASE

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
Yes
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
MSH Respirator,surgical

GMDN Terms

Code Name
57794 Surgical/medical respirator, non-antimicrobial, single-use

Identifiers

Type ID
Package 50051131499961
Primary 00051131499966
Unit of Use 00051131272330

Customer Contacts