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Remotion

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref 300-5200Model 08858251002902T3

by Stryker Corp.

Identity

Trade Name
Re-Motion EUDAMED
REMOTION FDA UDI
Generic Name
Surgical instrument/endoscope cleaning utensil, reusable FDA UDI
Device Name
RE-MOTION INSTRUMENTS - INTRA-OPERATIVE CLEANING INSTRUMENTATION - CLASS I - NON STERILE EUDAMED
Total Wrist, Cleaning Brush FDA UDI
Model / Reference
300-5200 EUDAMEDFDA UDI
08858251002902T3 EUDAMED
Description
Total Wrist, Cleaning Brush FDA UDI

Identifiers

Catalog Number
300-5200 FDA UDI
Primary DI / UDI-DI
00886385015118 EUDAMEDFDA UDI
Basic UDI-DI
08858251002902T3 EUDAMED
FDA Product Code
LXH FDA UDI
EMDN Code
P090380 WRIST PROSTHESES - ACCESSORIES EUDAMED
GMDN Term
Surgical instrument/endoscope cleaning utensil, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
888.4540 FDA UDI
Market of Registration
Netherlands EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

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

Yes

FDA UDI

Over-the-Counter

No

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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical instrument/endoscope cleaning utensil, reusable

Remotion by Stryker Corp. — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Surgical instrument/endoscope cleaning utensil, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stryker Corp.

Sources (2)

  • FDA UDI 4bb07267-e0fc-444e-8fa5-20b6134863f1 34 fields · synced Oct 8, 2026
  • EUDAMED c534df6e-0e43-444e-a288-c8ec59dd84d5 61 fields · synced Oct 8, 2026