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Invacare® Compass™ SPT™

FDA UDI

Class I (US FDA UDI)

by Invacare Corp.

Identity

Trade Name
Invacare® Compass™ SPT™ FDA UDI
Generic Name
Wheelchair, attendant/occupant-driven, rear-wheels-operated, collapsible FDA UDI
Device Name
Compass SPT FDA UDI
Model / Reference
SPT FDA UDI
Description
Compass SPT FDA UDI

Identifiers

Catalog Number
SPT FDA UDI
Primary DI / UDI-DI
00841447103110 FDA UDI
FDA Product Code
IOR FDA UDI
GMDN Term
Wheelchair, attendant/occupant-driven, rear-wheels-operated, collapsible FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3850 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

Yes

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

Category: Wheelchair, attendant/occupant-driven, rear-wheels-operated, collapsible

Invacare® Compass™ SPT™ by Invacare Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wheelchair, attendant/occupant-driven, rear-wheels-operated, collapsible.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Invacare Corp.

Sources (1)

  • FDA UDI 3864d80e-7972-411a-890c-a57eb638d0d6 35 fields · synced May 31, 2026