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Spectrum, Inc. 985-03652-000

by Spectrum Co.

Spectrum, Inc. 985-03652-000 (740440) is a Class I device made by Spectrum Co., listed in FDA GUDID since 14 Feb 2017 (UDI-DI 00850301007877), 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 Number00850301007877 UDI-DI Date14 Feb 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  • Withdrawn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
Spectrum, Inc.
Generic name
Stockinette
Model / Ref / Catalog
985-03652-000, 740440
Primary DI / UDI-DI
00850301007877
FDA product code
FQL
GMDN term
Stockinette
Device class
Class I
Regulation number
880.5780
GUDID distribution status
In Commercial Distribution
Sterilisation method
Ethylene Oxide
MRI safety
MR Safe

Related devices

Category: Stockinette

Similar devices in this category

Other devices filed under Stockinette.

Other devices from Spectrum Co.

See all devices from Spectrum Co. →

Properties

  • Supplied sterile
  • Sterilise before use
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (8, all answered No)