← Back to catalogue

Regard™

FDA UDI

Class I (US FDA UDI)

by Resource Optimization & Innovation, L.l.c.

Identity

Trade Name
Regard™ FDA UDI
Generic Name
Stockinette FDA UDI
Device Name
6" X 60" COTTON DOUBLE-PLY STERILE FDA UDI
Model / Reference
STCTK2PL6ST-REG FDA UDI
Description
6" X 60" COTTON DOUBLE-PLY STERILE FDA UDI

Identifiers

Catalog Number
STCTK2PL6ST-REG FDA UDI
Primary DI / UDI-DI
00326053121197 FDA UDI
FDA Product Code
FQL FDA UDI
GMDN Term
Stockinette FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5780 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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Stockinette

Regard™ by Resource Optimization & Innovation, L.l.c. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Stockinette.

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

Sources (1)

  • FDA UDI ede50246-f1ae-4849-acf6-f56ad09e58d2 34 fields · synced May 30, 2026