AccessGUDID - DEVICE: MEDLINE INDUSTRIES, INC. (10080196323692)

GUDID

Device Identifier (DI) Information

Brand Name: MEDLINE INDUSTRIES, INC.
Version or Model: MSC093005
Commercial Distribution Status: In Commercial Distribution
Catalog Number: MSC093005
Company Name: MEDLINE INDUSTRIES, INC.

Primary DI Number: 10080196323692
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 025460908 *Terms of Use

Device Description: PROTECTANT,SKIN,MARATHON,LIQUID

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
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":	Yes
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?
62535	Skin-cover sealant	A biodegradable, synthetic (e.g., cyanoacrylate) substance intended to be applied over a superficial wound to set and form a barrier to reduce skin exposure to external contaminants. Sometimes referred to as a liquid bandage, it is intended for use in the home or a clinical setting and may be intended as an alternative to a conventional skin-cover adhesive strip. After application, this device cannot be reused.	Active	false

[?]

FDA Product Code

Product Code	Product Code Name
KMF	Bandage, liquid

[?]

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K133443	000

Sterilization

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

Storage and Handling
Storage Environment Temperature: between 5 and 25 Degrees Celsius

[?]

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Alternative and Additional Identifiers Additional Identifiers

Package DI Number	Quantity per Package	Contains DI Package	Package Discontinue Date	Package Status	Package Type
30080196323696	10	10080196323692		In Commercial Distribution	CASE

Issuing Agency [?]	Secondary DI Number
No Secondary DIs found

Customer Contact

[?]

DEVICE: MEDLINE INDUSTRIES, INC. (10080196323692)

Device Identifier (DI) Information

Device Characteristics

GMDN

FDA Product Code

FDA Premarket Submission

Sterilization

Storage and Handling

Clinically Relevant Size

Device Record Status

Alternative and Additional Identifiers Additional Identifiers

Package DI

Secondary DI

Unit of Use DI

Direct Marking (DM)

Production Identifier(s) in UDI

Customer Contact