← Back to catalogue

Track

FDA UDIEUDAMED

Class I (US FDA UDI)

by Leggero Llc

Identity

Trade Name
Track FDA UDI
Generic Name
Attendant-only-propelled wheelchair, non-bariatric FDA UDI
Device Name
Pediatric pushchair. FDA UDI
Model / Reference
3002 FDA UDI
Description
Pediatric pushchair. FDA UDI

Identifiers

Primary DI / UDI-DI
B51430020 FDA UDI
FDA Product Code
INM FDA UDI
GMDN Term
Attendant-only-propelled wheelchair, non-bariatric FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3100 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

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: Attendant-only-propelled wheelchair, non-bariatric

Track by Leggero Llc — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Attendant-only-propelled wheelchair, non-bariatric.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Leggero Llc

Sources (2)

  • FDA UDI 11793882-970b-4b6f-b73a-d3d10b1b2ace 33 fields · synced Oct 7, 2026
  • EUDAMED 1 fields · synced Jun 4, 2026