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Ozark Trail Outdoor Equipment

FDA UDI

Class I (US FDA UDI)

by Walmart Stores

Identity

Trade Name
Ozark Trail Outdoor Equipment FDA UDI
Generic Name
Exudate-absorbent dressing, hydrophilic-gel, non-sterile FDA UDI
Device Name
Hydrocolloid Gel Blister Cushions, one size, 1.65 IN x 2.67 IN (42 mm x 68 mm) FDA UDI
Model / Reference
017276235937 FDA UDI
Description
Hydrocolloid Gel Blister Cushions, one size, 1.65 IN x 2.67 IN (42 mm x 68 mm) FDA UDI

Identifiers

Primary DI / UDI-DI
00017276235937 FDA UDI
FDA Product Code
NAD FDA UDI
GMDN Term
Exudate-absorbent dressing, hydrophilic-gel, non-sterile FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4020 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

Yes

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

Category: Exudate-absorbent dressing, hydrophilic-gel, non-sterile

Ozark Trail Outdoor Equipment by Walmart Stores — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Exudate-absorbent dressing, hydrophilic-gel, non-sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Walmart Stores

Sources (1)

  • FDA UDI 199fcdb1-3cf7-4a86-9b8b-740d7a75c298 33 fields · synced May 29, 2026