AccessGUDID - DEVICE: ACTICOAT FLEX7 2.5CMX60CM CTN OF 5 (00040565125275)

GUDID

Device Identifier (DI) Information

Brand Name: ACTICOAT FLEX7 2.5CMX60CM CTN OF 5
Version or Model: 66800545
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 66800545, 66800544
Company Name: SMITH & NEPHEW MEDICAL LIMITED

Primary DI Number: 00040565125275
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 216344051 *Terms of Use

Device Description: Silver coated anti-microbial barrier dressing

Device Characteristics

What MRI safety information does the labeling contain?	MR Unsafe
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	Yes
Prescription Use (Rx):	Yes
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
47042	Wound-nonadherent dressing, absorbent, antimicrobial	A wound covering typically in the form of a multi-layered pad having a material on its skin-contact surface that prevents adherence to the wound bed (e.g., soft silicone), thereby decreasing the potential for wound trauma, and that contains an antimicrobial agent [e.g., silver (Ag), honey]. It is used to absorb blood and exudates from the wound, while protecting the wound from external contamination and maintaining a moist internal environment. It may be used as a primary or secondary dressing with other wound-care products to treat chronic and postoperative wounds, burns, ulcers, abrasions, cuts, or puncture sites. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
FRO	Dressing, Wound, Drug

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K083113	000

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: Yes
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 78005e5f-dda7-4b93-8ab6-9ecd740ecd3b
Public Version Date: September 07, 2023
Public Version Number: 6
DI Record Publish Date: May 15, 2020

Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]

Package DI Number	Quantity per Package	Contains DI Package	Package Status	Package Type
00040565125282	5	00040565125275	In Commercial Distribution	Carton
30040565125283	10	00040565125282	In Commercial Distribution	Case
00040565125268	5	00040565125275	In Commercial Distribution	Carton 66800544
30040565125269	10	00040565125268	In Commercial Distribution	Case 66800544