Skip to content

PremierPro 3821

by Prestige Ameritech

PremierPro 3821 is a device made by Prestige Ameritech, listed in FDA GUDID since 5 Apr 2019 (UDI-DI 00811220031732), 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 Number00811220031732 UDI-DI Date5 Apr 2019ListedStatusListed 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  • Withdrawn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
PremierPro
Generic name
Blanket warming cabinet, dry-heat
Model / Ref / Catalog
3821
Primary DI / UDI-DI
00811220031732
FDA product code
DJW
GMDN term
Blanket warming cabinet, dry-heat
GUDID distribution status
In Commercial Distribution
MRI safety
MR Safe

Related devices

Category: Blanket warming cabinet, dry-heat

Other devices from Prestige Ameritech

See all devices from Prestige Ameritech →

Properties

  • Single use
Other properties (14, all answered No)