FDA UDI In Commercial Distribution 🇺🇸 United States

3M™ Tegaderm™

DI: 04046719388936 · Model: 1683 · 3M COMPANY
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
100

Basic Information

Brand Name
3M™ Tegaderm™
Primary DI
04046719388936
Version / Model
1683
Catalog Number
1683
Company Name
3M COMPANY
Labeler DUNS
830016148
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2018-09-24
Public Version
2
Public Version Date
2021-12-22
Public Version Status
Update
Public Device Record Key
f6e20694-47e7-4a72-b351-a0be7549a411

Device Description

3M(TM) Tegaderm(TM) IV Advanced Securement Dressing 1683

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
Yes
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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KMK DEVICE, INTRAVASCULAR CATHETER SECUREMENT

GMDN Terms

Code Name
58301 Synthetic polymer semi-permeable film dressing, adhesive

Identifiers

Type ID
Package 50707387582758
Primary 04046719388936
Unit of Use 00707387582753

Customer Contacts