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Dalton Primechair

FDA UDI

Class II (US FDA UDI)

by Dalton Medical Corp.

Identity

Trade Name
DALTON PRIMECHAIR FDA UDI
Generic Name
Electric-motor-driven wheelchair, attendant-controlled FDA UDI
Device Name
PRIMECHAIR MID-WHEEL DRIVE, WT. LIMIT 300 lbs. W/20" CAPTAIN SEAT FDA UDI
Model / Reference
PC-MP3CM3AR20 FDA UDI
Description
PRIMECHAIR MID-WHEEL DRIVE, WT. LIMIT 300 lbs. W/20" CAPTAIN SEAT FDA UDI

Identifiers

Primary DI / UDI-DI
00815027012666 FDA UDI
FDA Product Code
ITI FDA UDI
GMDN Term
Electric-motor-driven wheelchair, attendant-controlled FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.3860 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

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: Electric-motor-driven wheelchair, attendant-controlled

Dalton Primechair by Dalton Medical Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electric-motor-driven wheelchair, attendant-controlled.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dalton Medical Corp.

Sources (1)

  • FDA UDI 164df9e3-010b-44a3-bc64-211a967a6f1d 34 fields · synced Jun 1, 2026