← 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
Surgical cap, single-use FDA UDI
Device Name
SURGEON CAP WITH BACK ELASTIC, REGULAR SIZE, SMS/POLYPROPYLENE, BLUE, DISP, NS, LF FDA UDI
Model / Reference
SRGCPELS1-REG FDA UDI
Description
SURGEON CAP WITH BACK ELASTIC, REGULAR SIZE, SMS/POLYPROPYLENE, BLUE, DISP, NS, LF FDA UDI

Identifiers

Catalog Number
SRGCPELS1-REG FDA UDI
Primary DI / UDI-DI
00326053119255 FDA UDI
FDA Product Code
FYF FDA UDI
GMDN Term
Surgical cap, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4040 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical cap, single-use

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 Surgical cap, 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

Sources (1)

  • FDA UDI 8bb28e2c-0583-4a34-a334-b25155da811e 34 fields · synced May 30, 2026