← Back to catalogue

Royla Flush

FDA UDI

Class I (US FDA UDI)

by Royal Knit, Inc.

Identity

Trade Name
ROYLA FLUSH FDA UDI
Generic Name
Stump sock FDA UDI
Device Name
(8"-12") Double Fleece 2 Ply White X-Large Rubberized Hole FDA UDI
Model / Reference
GOBRF235-01-14 FDA UDI
Description
(8"-12") Double Fleece 2 Ply White X-Large Rubberized Hole FDA UDI

Identifiers

Catalog Number
GOBRF235-01-14 FDA UDI
Primary DI / UDI-DI
GOBRF23501140 FDA UDI
FDA Product Code
FQL FDA UDI
GMDN Term
Stump sock 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

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: Stump sock

Royla Flush by Royal Knit, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Stump sock.

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
Royal Knit, Inc.

Sources (1)

  • FDA UDI c8503c58-dee7-4b79-a066-a2a5b0085b19 34 fields · synced May 31, 2026