Device
3M™ Tegaderm™ I.V. Advanced Securement Dressing 1683NS, 2 1/2 Inches X 23/4Inches (6,5cm x 7cm), 2500 EA/Case
Manufacturer
3M Deutschland GmbH
Model: 1683NS Catalog: 1683NS DI: 50707387818079 Status: New MRI: Labeling does not contain MRI Safety Information Single-use: Yes Rx: No OTC: No
First Published: 2026-05-08 Current Version: 2026-05-18
Description
3M™ Tegaderm™ I.V. Advanced Securement Dressing 1683NS, 2 1/2 Inches X 23/4Inches (6,5cm x 7cm), 2500 EA/Case
Sterilization
Method Types - Sterilization Method: Ethylene Oxide
Device Sterile: No
Sterilization Prior To Use: Yes
Regulatory & Distribution
Record Status: Published
Version Number: 1
Record Key: 3ab7db73-1cce-421a-8dbc-e1ee1d8c608e
Distribution Status: In Commercial Distribution
DUNS Number: 315731711
Device Count: 2500
DM Exempt: No
Premarket Exempt: Yes
HCT/P: No
Kit: No
Combination Product: No
Lot/Batch Tracked: Yes
Serial Number Tracked: No
Manufacturing Date Tracked: Yes
Expiration Date Tracked: Yes
Donation ID Number Tracked: No
Labeled Contains NRL: No
Labeled No NRL: Yes
Identifiers
Item #1 - Device ID: 00707387818074
Item #1 - Device ID Type: Unit of Use
Item #1 - Device ID Issuing Agency: GS1
Item #2 - Device ID: 50707387818079
Item #2 - Device ID Type: Primary
Item #2 - Device ID Issuing Agency: GS1
GMDN
Code: 58301
Name: Synthetic polymer semi-permeable film dressing, adhesive
Definition:
A transparent, semi-permeable (i.e., impermeable to fluids, permeable to vapours and gases) covering applied to wounded or diseased tissue intended to provide protection (e.g., from dirt, water) and/or promote healing. It is a thin, clear film made of synthetic polymer material that is covered on one side with a pressure-sensitive adhesive. It may be applied directly to tissue or used in combination with other dressings (e.g., gauze) to protect postsurgical incisions and minor wounds (e.g., cuts, scrapes, burns, skin tears, blisters). It may also be used to secure to skin other devices such as vascular catheters, infusion ports, or tubing. This is a single-use device.
FDA Product Codes
KMK
DEVICE, INTRAVASCULAR CATHETER SECUREMENT