FDA UDI In Commercial Distribution 🇺🇸 United States

3M™

DI: 30707387234806 · Model: 2181 · 3M COMPANY
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
102

Basic Information

Brand Name
3M™
Primary DI
30707387234806
Version / Model
2181
Catalog Number
2181
Company Name
3M COMPANY
Labeler DUNS
830016148
Distribution Status
In Commercial Distribution
Device Count in Pkg
102
Record Status
Published
Publish Date
2018-09-26
Public Version
1
Public Version Date
2018-10-29
Public Version Status
New
Public Device Record Key
0e884281-30b2-4555-aa31-f925e852e70d

Device Description

3M™ Double Stick Discs 2181, 6 BAGS/CASE 4-5/16"X 2"

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
Yes
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
LDE STETHOSCOPE, MANUAL

GMDN Terms

Code Name
13755 Mechanical stethoscope

Identifiers

Type ID
Package 50707387234800
Primary 30707387234806
Unit of Use 00707387234805

Customer Contacts