FDA UDI In Commercial Distribution 🇺🇸 United States

3M™ ESPE™

DI: 30605861032217 · Model: 7522S · 3M COMPANY
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
200

Basic Information

Brand Name
3M™ ESPE™
Primary DI
30605861032217
Version / Model
7522S
Catalog Number
7522S
Company Name
3M COMPANY
Labeler DUNS
830016148
Distribution Status
In Commercial Distribution
Device Count in Pkg
200
Record Status
Published
Publish Date
2018-09-24
Public Version
2
Public Version Date
2018-11-08
Public Version Status
Update
Public Device Record Key
d1a6fabf-e11b-40fb-8efa-5f661f6e402c

Device Description

3M™ ESPE™ Disposable Mini-Sponge Applicators, 7522S

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
Yes
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
KXR APPLICATOR, RESIN

GMDN Terms

Code Name
35697 Dental material application tool, single-use

Identifiers

Type ID
Package 50605861032211
Primary 30605861032217
Unit of Use 00605861032216

Customer Contacts