← Back to catalogue

3M™ Tegaderm™

FDA UDI

Class U (US FDA UDI)

by 3m Company

Identity

Trade Name
3M™ Tegaderm™ FDA UDI
Generic Name
Antimicrobial synthetic polymer semi-permeable film dressing, adhesive FDA UDI
Device Name
3M™ Tegaderm™ CHG Chlorhexidine Gluconate I.V. Port Dressing, 1665NS, 4-3/4 in x 4-3/4 in, Non Sterile, 250/Case FDA UDI
Model / Reference
1665NS FDA UDI
Description
3M™ Tegaderm™ CHG Chlorhexidine Gluconate I.V. Port Dressing, 1665NS, 4-3/4 in x 4-3/4 in, Non Sterile, 250/Case FDA UDI

Identifiers

Catalog Number
1665NS FDA UDI
Primary DI / UDI-DI
50707387810226 FDA UDI
FDA Product Code
FRO FDA UDI
GMDN Term
Antimicrobial synthetic polymer semi-permeable film dressing, adhesive FDA UDI

Classification

Device Class
U FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

Yes

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Antimicrobial synthetic polymer semi-permeable film dressing, adhesive

3M™ Tegaderm™ by 3m Company — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Antimicrobial synthetic polymer semi-permeable film dressing, adhesive.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
3m Company

Sources (1)

  • FDA UDI 75455bc8-1b28-4039-a54c-151369b38b05 35 fields · synced May 30, 2026