← Back to catalogue

Case Tray for Nicholson Shoulder Extractor

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 9006-TRAY

by Innomed, Inc.

Identity

Trade Name
Case Tray for Nicholson Shoulder Extractor EUDAMED
Innomed, Inc. FDA UDI
Generic Name
Device sterilization/disinfection container, reusable FDA UDI
Device Name
Tray EUDAMED
Case Tray Nicholson Shoulder Extractor FDA UDI
Model / Reference
9006-TRAY EUDAMEDFDA UDI
Description
Case Tray Nicholson Shoulder Extractor FDA UDI

Identifiers

Catalog Number
9006-TRAY FDA UDI
Primary DI / UDI-DI
00840277115553 EUDAMEDFDA UDI
Basic UDI-DI
8402771INNOTRAY01EX EUDAMED
Direct Marketing DI
00840277115553 EUDAMED
FDA Product Code
FSM FDA UDI
EMDN Code
S010499 STERILISATION CONTAINERS - OTHER EUDAMED
GMDN Term
Device sterilization/disinfection container, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
878.4800 FDA UDI
Market of Registration
Germany 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

No

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

No

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

Case Tray for Nicholson Shoulder Extractor by Innomed, 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
Innomed, Inc.
EUDAMED SRN
US-MF-000014761
Authorised Representative
MediMark Europe Sarl. FR-AR-000000182

Sources (2)

  • EUDAMED d0b5f108-308e-48e9-9773-d6f371d36f41 61 fields · synced Aug 3, 2026
  • FDA UDI dd58fec9-6c37-4ac9-804f-57de37bee07e 34 fields · synced May 30, 2026