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Discovery Base Unit

FDA UDI

Class II (US FDA UDI)

by SRS Medical Systems, Inc.

Identity

Trade Name
Discovery Base Unit FDA UDI
Generic Name
Biomechanical function analysis system, motion-tracking FDA UDI
Model / Reference
900-010 FDA UDI

Identifiers

Primary DI / UDI-DI
00890477000166 FDA UDI
510(k) Number
K063447 FDA UDI
FDA Product Code
HCC FDA UDI
IKN FDA UDI
GMDN Term
Biomechanical function analysis system, motion-tracking FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.5050 FDA UDI
890.1375 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

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

No

FDA UDI

Category: ElectromyographKinesiology/electromyographic sensor setElectronic goniometer/kinesiology sensorBiofeedback system application software

Discovery Base Unit by SRS Medical Systems, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Biomechanical function analysis system, motion-tracking.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b566d406-e11b-4a9c-bd5b-006fbe5af1a0 33 fields · synced Jun 1, 2026