EliA Symphony Well DECC055080

EliA Symphony Well DECC055080 is a Class II device made by Phadia AB, listed in FDA GUDID since 23 Sep 2016 (UDI-DI 07333066014593), registry data as of 12 Nov 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

Source GUDID, synced 12 Nov 2026.

Regulatory status

as of registry sync 12 Nov 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number07333066014593 UDI-DI	Date23 Sep 2016Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 07333066014593

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: EliA Symphony Well
Generic name: Multiple antinuclear antibody (ANA) IVD, kit, fluorescent immunoassay
Model / Ref / Catalog: DECC055080

Primary DI / UDI-DI: 07333066014593
FDA product code: LLL
GMDN term: Multiple antinuclear antibody (ANA) IVD, kit, fluorescent immunoassay

Device class: Class II
Regulation number: 866.5100
GUDID distribution status: In Commercial Distribution

Similar devices in this category

Other devices filed under Multiple antinuclear antibody (ANA) screening IVD, kit, fluorescent immunoassay.

Other devices from Phadia AB

EliA CTD 13 Screen Well DECC066610

Class II
EliA Stool Extraction Buffer plus 83-1187-01

Class I
EliA Stool Extraction Kit plus 14-6665-01

Class I
EliA Celikey IgA Well DECC066170

Class II

See all devices from Phadia AB →

Properties

Prescription use
Lot / batch number
Expiration date

Other properties (12, all answered No)