← Back to catalogue

Royal Open Toe

EUDAMEDFDA UDI

Class I (EU MDR)

Ref SRK1P-23-12

by Royal Knit, Inc

Identity

Trade Name
Royal Open Toe EUDAMED
ROYAL DOUBLE FLEECE FDA UDI
Generic Name
Stump sock FDA UDI
Device Name
Royal Flush EUDAMED
(10"-14") Double Fleece 1 Ply White Large Open Toe FDA UDI
Model / Reference
SRK1P-23-12 EUDAMEDFDA UDI
Description
(10"-14") Double Fleece 1 Ply White Large Open Toe FDA UDI

Identifiers

Catalog Number
SRK1P-23-12 FDA UDI
Primary DI / UDI-DI
+G296SRK1P23120 EUDAMED
G296SRK1P23120 FDA UDI
Basic UDI-DI
++G296PROSTHEICSOCKSQD EUDAMED
FDA Product Code
FQL FDA UDI
EMDN Code
Y090327 SOCKS FOR PROSTHESES EUDAMED
GMDN Term
Stump sock FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
880.5780 FDA UDI
Market of Registration
Denmark EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

Royal Open Toe by Royal Knit, Inc. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Royal Knit, Inc
EUDAMED SRN
US-MF-000004427
Authorised Representative
Code of Practice AB SE-AR-000003002

Sources (2)

  • EUDAMED 78a49390-5835-40d2-8738-7d21c6791f4d 61 fields · synced Jul 29, 2026
  • FDA UDI 52b3abe3-a460-4bf6-8e8f-c38c9d0bdaec 34 fields · synced May 30, 2026