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Aesculap InOS®

EUDAMEDFDA UDI

Class I (EU MDR)

Ref JG378

by Aesculap AG

Identity

Trade Name
Aesculap InOS® EUDAMED
AESCULAP FDA UDI
Generic Name
Surgical instrument/implant rack FDA UDI
Device Name
Plastic components for baskets EUDAMED
CUSHIONING RACK 113X18X21MM FDA UDI
Model / Reference
JG378 EUDAMEDFDA UDI
Description
CUSHIONING RACK 113X18X21MM FDA UDI

Identifiers

Catalog Number
JG378 FDA UDI
Primary DI / UDI-DI
04046955194896 EUDAMEDFDA UDI
Basic UDI-DI
40392390000005472J EUDAMED
Direct Marketing DI
04046955194896 EUDAMED
FDA Product Code
FSM FDA UDI
EMDN Code
S010401 TRAYS, BASKETS, TUBS FOR STERILISATION AND THEIR COMPONENTS EUDAMED
GMDN Term
Surgical instrument/implant rack 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

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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Instrument tray, reusable

Aesculap InOS® by Aesculap AG — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Instrument tray, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Aesculap AG
EUDAMED SRN
DE-MF-000005504

Sources (2)

  • EUDAMED eb51a10a-eb68-47c7-afe6-77d32c3dfdb8 61 fields · synced Jun 18, 2026
  • FDA UDI 8e5eef6e-d70d-4232-8e0c-6165097f4405 35 fields · synced May 30, 2026