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Invacare 9805P Hydraulic Patient Lift

FDA UDI

Class I (US FDA UDI)

by Invacare Corp.

Identity

Trade Name
Invacare 9805P Hydraulic Patient Lift FDA UDI
Generic Name
Mobile patient lifting system, manual FDA UDI
Device Name
KIT 1 EA 9805P 1 EA R111 FDA UDI
Model / Reference
9805P-R111-KIT FDA UDI
Description
KIT 1 EA 9805P 1 EA R111 FDA UDI

Identifiers

Primary DI / UDI-DI
00841447115014 FDA UDI
FDA Product Code
FSA FDA UDI
GMDN Term
Mobile patient lifting system, manual FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5510 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

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: Mobile patient lifting system, manual

Invacare 9805P Hydraulic Patient Lift by Invacare Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Mobile patient lifting system, manual.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Invacare Corp.

Sources (1)

  • FDA UDI 0090a2ff-4398-4bd7-b7ed-93a04e33b77f 34 fields · synced Jun 8, 2026