Skip to content

Wolf 982-03715-000

by Spectrum Co.

Wolf 982-03715-000 (956920WOL) is a Class II device made by Spectrum Co., listed in FDA GUDID since 30 Jan 2017 (UDI-DI 00850301007020), 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 Number00850301007020 UDI-DI Date30 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  • Withdrawn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
Wolf
Generic name
Medical equipment/instrument drape, single-use
Model / Ref / Catalog
982-03715-000, 956920WOL
Primary DI / UDI-DI
00850301007020
FDA product code
KKX
GMDN term
Medical equipment/instrument drape, single-use
Device class
Class II
Regulation number
878.4370
GUDID distribution status
In Commercial Distribution
Sterilisation method
Ethylene Oxide
MRI safety
MR Safe

Similar devices in this category

Other devices filed under Medical equipment/instrument drape, single-use.

Other devices from Spectrum Co.

See all devices from Spectrum Co. →

Properties

  • Supplied sterile
  • Sterilise before use
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)