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careGARD

FDA UDI

Class I (US FDA UDI)

by Extremity Care, Llc

Identity

Trade Name
careGARD FDA UDI
Generic Name
Synthetic polymer semi-permeable film dressing, adhesive FDA UDI
Device Name
careGARD A Sterile Bordered Gauze Dressing Tape 4" x 4" Pad 2.5"X 2.5" FDA UDI
Model / Reference
EC002 FDA UDI
Description
careGARD A Sterile Bordered Gauze Dressing Tape 4" x 4" Pad 2.5"X 2.5" FDA UDI

Identifiers

Primary DI / UDI-DI
00850003042190 FDA UDI
FDA Product Code
NAC FDA UDI
GMDN Term
Synthetic polymer semi-permeable film dressing, adhesive FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4018 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Width — 2.5 Inch FDA UDI
Length — 2.5 Inch FDA UDI

Category: Synthetic polymer semi-permeable film dressing, adhesive

careGARD by Extremity Care, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Extremity Care, Llc

Sources (1)

  • FDA UDI 5b7645cb-c6bd-4f52-87ca-d1bda7902655 34 fields · synced May 31, 2026