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Leader 6155717

by Cardinal Health 110, Inc.

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 26 Oct 2026. What this means

Regulatory status

as of registry sync 26 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00096295146639 UDI-DI Date9 Oct 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Leader
Generic Name
Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial
Model / Ref / Catalog
6155717
Primary DI / UDI-DI
00096295146639
FDA Product Code
NAD
GMDN Term
Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial
Device Class
Class I
Regulation Number
878.4020
GUDID distribution status
In Commercial Distribution
Size
Width — 1.14 Inch
Length — 2.32 Inch

Overview

AI-generated summary, 26 Oct 2026

Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data above is the record.

The LEADER 6155717 is a Dressing, Wound, Occlusive. It is an exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial. This device is a wound covering, typically made of a hydrocolloid, hydrofibre, chitosan or alginate, intended to produce a water-absorbent gel upon contact with wound exudate. It is provided sterile and is for single use only. The device is available in a width of 1.14 Inch and a length of 2.32 Inch.

This device is classified as Class I. It is regulated under 878.4020 and assigned product code NAD. The filing category is General, Plastic Surgery. Labeling does not contain MRI Safety Information.

Other devices from Cardinal Health 110, Inc.

See all devices from Cardinal Health 110, Inc. →

Questions

AI-generated answers, 26 Oct 2026

Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data above is the record.

  • What is the LEADER 6155717?

    It is recorded under the device type "Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial". A wound covering, typically made of a hydrocolloid, hydrofibre, chitosan or alginate (salts and acids extracted from seaweed), intended to produce a water-absorbent gel upon contact with wound exudate; it does not contain an antimicrobial agent. FDA lists it under the product name "Dressing, Wound, Occlusive". It is recorded as Class I.

  • What are the product code and regulation of the LEADER 6155717?

    FDA records the LEADER 6155717 under product code NAD and regulation number 878.4020.

  • Who makes the LEADER 6155717?

    Cardinal Health 110, Inc. is the manufacturer on record for the LEADER 6155717.

Properties

  • Sterile
  • Single Use
  • Over-the-Counter
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (7)

  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No