FDA UDI Not in Commercial Distribution 🇺🇸 United States

3M™ ESPE™

DI: 30348878600030 · Model: 12138 · 3M COMPANY
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
9

Basic Information

Brand Name
3M™ ESPE™
Primary DI
30348878600030
Version / Model
12138
Catalog Number
12138
Company Name
3M COMPANY
Labeler DUNS
830016148
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
9
Record Status
Published
Publish Date
2018-10-31
Public Version
3
Public Version Date
2023-01-17
Public Version Status
Update
Public Device Record Key
738b3f8f-139b-4882-acd9-11f1b4e58f50
Distribution End Date
2023-01-16

Device Description

3M™ ESPE™ Xerostomia Relief Spray, Sample Kit, 12138

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
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
LFD SALIVA, ARTIFICIAL

GMDN Terms

Code Name
47276 Oropharyngeal mucosa protection material

Identifiers

Type ID
Primary 30348878600030
Unit of Use 00348878600039

Customer Contacts