← Back to catalogue

PrimaCare®

FDA UDI

Class I (US FDA UDI)

by Derma Sciences Canada, Inc

Identity

Trade Name
PrimaCare® FDA UDI
Generic Name
Skin treatment/dressing-supportive limb/finger bandage, single-use FDA UDI
Device Name
4 in X 5 yards premium elastic bandage with removable clips. FDA UDI
Model / Reference
71404LF FDA UDI
Description
4 in X 5 yards premium elastic bandage with removable clips. FDA UDI

Identifiers

Catalog Number
DUP71404LF FDA UDI
Primary DI / UDI-DI
00809958078419 FDA UDI
FDA Product Code
FQM FDA UDI
GMDN Term
Skin treatment/dressing-supportive limb/finger bandage, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5075 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

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Skin treatment/dressing-supportive limb/finger bandage, single-use

PrimaCare® by Derma Sciences Canada, Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Skin treatment/dressing-supportive limb/finger bandage, single-use.

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
Derma Sciences Canada, Inc

Sources (1)

  • FDA UDI 7e199e42-a0c6-4159-9f08-c6ca322c0f07 36 fields · synced Jun 8, 2026