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Case Lid SOS Half

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 2022-LID-A

by Innomed, Inc.

Identity

Trade Name
Case Lid SOS Half EUDAMED
Innomed, Inc. FDA UDI
Generic Name
Device sterilization/disinfection container, reusable FDA UDI
Device Name
Tray EUDAMED
Case Lid SOS Half FDA UDI
Model / Reference
2022-LID-A EUDAMEDFDA UDI
Description
Case Lid SOS Half FDA UDI

Identifiers

Catalog Number
2022-LID-A FDA UDI
Primary DI / UDI-DI
00840277129925 EUDAMEDFDA UDI
Basic UDI-DI
8402771INNOTRAY01EX EUDAMED
Direct Marketing DI
00840277129925 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 Lid SOS Half 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

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Manufacturer

Manufacturer
Innomed, Inc.
EUDAMED SRN
US-MF-000014761
Authorised Representative
MediMark Europe Sarl. FR-AR-000000182

Sources (2)

  • EUDAMED 6637a494-6af7-49e1-be53-9b9ad70ab00e 61 fields · synced Jun 18, 2026
  • FDA UDI 93dbe4fa-fa22-4837-9a45-fda5f1765161 34 fields · synced May 30, 2026