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Replacement Base for Invacare 9805 Hydraulic Lift

FDA UDI

Class I (US FDA UDI)

by Invacare Corp.

Identity

Trade Name
Replacement Base for Invacare 9805 Hydraulic Lift FDA UDI
Generic Name
Patient lifting system bath chair FDA UDI
Device Name
Replacement Base for Invacare 9805 Hydraulic Lift FDA UDI
Model / Reference
9884 FDA UDI
Description
Replacement Base for Invacare 9805 Hydraulic Lift FDA UDI

Identifiers

Catalog Number
9884 FDA UDI
Primary DI / UDI-DI
00841447102670 FDA UDI
FDA Product Code
FSA FDA UDI
GMDN Term
Patient lifting system bath chair 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

No

FDA UDI

Category: Patient lifting system bath chair

Replacement Base for Invacare 9805 Hydraulic Lift by Invacare Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Patient lifting system bath chair.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Invacare Corp.

Sources (1)

  • FDA UDI cab5b51a-ce53-4fa9-9150-1f592164530c 35 fields · synced May 30, 2026