Skip to content

Amplim XA202

by Amplim, LLC

Amplim XA202 is a Class I device made by Amplim, LLC, listed in FDA GUDID since 28 May 2023 (UDI-DI 00810477025518), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00810477025518 UDI-DI Date28 May 2023ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Amplim
Generic name
Breast pump, manual
Model / reference
XA202
Primary DI / UDI-DI
00810477025518
FDA product code
HGY
GMDN term
Breast pump, manual
Device class
Class I
Regulation number
884.5150
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code HGY (Pump, Breast, Non-Powered).

Other devices from Amplim, LLC

See all devices from Amplim, LLC →

Properties

  • Convenience kit
  • Lot / batch number
Other properties (13, all answered No)