← Back to catalogue

MD 62 System Transmitter

EUDAMEDFDA UDI

Class I (EU MDR)

Ref MDWL2_B1J1TXModel MDWL2_B1J1TX

by Rocoto Inc.

Identity

Trade Name
MD 62 System Transmitter EUDAMED
Amimon FDA UDI
Generic Name
Medical image management system FDA UDI
Device Name
MD 62 System Transmitter EUDAMED
MD62 Tx device FDA UDI
Model / Reference
MDWL2_B1J1TX EUDAMED
MD62 Tx device - MDWL2_B1J1TX FDA UDI
Description
MD62 Tx device FDA UDI

Identifiers

Catalog Number
MDWL2_B1J1TX FDA UDI
Primary DI / UDI-DI
00860014100604 EUDAMEDFDA UDI
Basic UDI-DI
008600141006047X EUDAMED
FDA Product Code
OUG FDA UDI
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED
GMDN Term
Medical image management system FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
880.6310 FDA UDI
Market of Registration
Austria 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Device sterilization/disinfection container, reusable

MD 62 System Transmitter by Rocoto Inc. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Device sterilization/disinfection container, reusable.

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
Rocoto Inc.
EUDAMED SRN
US-MF-000045904
Authorised Representative
CEpartner4U NL-AR-000000111

Sources (2)

  • EUDAMED 4644cfe2-eb03-47eb-99ba-ee4dbb4de7ba 61 fields · synced Jul 16, 2026
  • FDA UDI ee5740a7-123d-4cea-8df8-cb1c4bfa547a 34 fields · synced May 30, 2026