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Modus

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref M-6721

by Medartis Inc.

Identity

Trade Name
Implant and Instrument Case 120x20mm EUDAMED
MODUS FDA UDI
Generic Name
Device sterilization/disinfection container, reusable FDA UDI
Device Name
Container EUDAMED
Implant and Instrument Case 120 x 20 mm FDA UDI
Model / Reference
M-6721 EUDAMEDFDA UDI
Description
Implant and Instrument Case 120 x 20 mm FDA UDI

Identifiers

Catalog Number
M-6721 FDA UDI
Primary DI / UDI-DI
07630037856269 EUDAMEDFDA UDI
Basic UDI-DI
76300378000NY EUDAMED
510(k) Number
K230971 FDA UDI
FDA Product Code
HRS FDA UDI
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED
GMDN Term
Device sterilization/disinfection container, reusable FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
888.3030 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

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Device sterilization/disinfection container, reusable

Modus by Medartis Inc. — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Device sterilization/disinfection container, reusable.

Cleared under the same submission

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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

Manufacturer

Manufacturer
Medartis Inc.

Sources (2)

  • FDA UDI f2695a7a-adbc-4e19-a97e-9bc69aad8c81 35 fields · synced Jun 19, 2026
  • EUDAMED 713b2175-519f-473e-8e83-c8d869026bae 61 fields · synced Jun 19, 2026