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LokomatNanos V1.2 220V

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 31000

by Hocoma AG

Identity

Trade Name
LokomatNanos V1.2 220V EUDAMED
Lokomat FDA UDI
Generic Name
Treadmill/elliptical gait rehabilitation system FDA UDI
Device Name
LokomatNanos V1.2 EUDAMED
Model / Reference
31000 EUDAMED
Nanos V1.2 FDA UDI

Identifiers

Catalog Number
31000 FDA UDI
Primary DI / UDI-DI
07640174660209 EUDAMEDFDA UDI
Basic UDI-DI
B-07640174660209 EUDAMED
FDA Product Code
BXB FDA UDI
EMDN Code
N010299 NEUROLOGIC PHYSIOTHERAPHY DEVICES - OTHER EUDAMED
GMDN Term
Treadmill/elliptical gait rehabilitation system FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
890.5380 FDA UDI
Commercial Distribution
Not 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

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

LokomatNanos V1.2 220V by Hocoma Ag — Class IIa — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hocoma AG
EUDAMED SRN
CH-MF-000014672
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (2)

  • EUDAMED 348bf0c8-67b0-44a9-84b5-3b419a22f072 61 fields · synced Jul 21, 2026
  • FDA UDI bace36ce-8cee-4b36-93be-7a185b0d2a40 34 fields · synced May 30, 2026