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Lode B.V.

FDA UDI

Class I (US FDA UDI)

by Lode B.V.

Identity

Trade Name
Lode B.V. FDA UDI
Generic Name
Cardiopulmonary stress exercise treadmill FDA UDI
Device Name
938903 Valiant 2 rehab XL FDA UDI
Model / Reference
938903 FDA UDI
Description
938903 Valiant 2 rehab XL FDA UDI

Identifiers

Primary DI / UDI-DI
08717524640088 FDA UDI
FDA Product Code
IOL FDA UDI
GMDN Term
Cardiopulmonary stress exercise treadmill FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.5380 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Cardiopulmonary stress exercise treadmill

Lode B.V. by Lode B.V. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cardiopulmonary stress exercise treadmill.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Lode B.V.

Sources (1)

  • FDA UDI e8c2133d-73a8-4a14-a57e-7f35c93e93cd 33 fields · synced May 30, 2026