Skip to content

Beesure BE1251

by Ascend Eagle Incorporated

Beesure BE1251 is a Class II device made by Ascend Eagle Incorporated, listed in FDA GUDID since 3 Jan 2017 (UDI-DI 10817508020075), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10817508020075 UDI-DI Date3 Jan 2017ListedStatusListed 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  • Withdrawn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
Beesure
Generic name
Sterilization packaging, single-use
Model / reference
BE1251
Description
Beesure Sterilization Pouch 200 /BAG , 5 1/4" x 11"
Primary DI / UDI-DI
10817508020075
FDA product code
FRG
GMDN term
Sterilization packaging, single-use
Device class
Class II
Regulation number
880.6850
GUDID distribution status
In Commercial Distribution

Related devices

Category: Sterilization packaging, single-use

Other devices from Ascend Eagle Incorporated

See all devices from Ascend Eagle Incorporated →

Properties

  • Single use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (11, all answered No)