AccessGUDID - DEVICE: CURAD (00197344099026)

GUDID

Device Identifier (DI) Information

Brand Name: CURAD
Version or Model: NON270603
Commercial Distribution Status: In Commercial Distribution
Catalog Number: NON270603
Company Name: MEDLINE INDUSTRIES, INC.

Primary DI Number: 00197344099026
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 4
Labeler D-U-N-S® Number*: 025460908 *Terms of Use

Device Description: TAPE,ELASTIC,FOAM,CURAD,3X5.5YD,LF,24/C

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):	No
Over the Counter (OTC):	Yes
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?
66337	Limb immobilization/support skin adhesive tape	A flexible band of fabric, plastic, or other material intended to noninvasively adhere to the skin surface to immobilize a joint and/or support a limb. It may be referred to as sports tape, functional tape, or kinesiology tape and is coated on one side with a pressure-sensitive adhesive and designed with a lower potential for producing an allergic reaction (i.e., hypoallergenic). This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
KGX	Tape and bandage, adhesive

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: Yes CLOSE

Sterilization

Device Packaged as Sterile: No
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: 70bc6b70-9fde-49b7-beb4-2a4eb891d9f0
Public Version Date: April 23, 2025
Public Version Number: 1
DI Record Publish Date: April 15, 2025

Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]

Package DI Number	Quantity per Package	Contains DI Package	Package Discontinue Date	Package Status	Package Type
40197344099024	6	00197344099026		In Commercial Distribution	CS

Secondary DI

[?]

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

Unit of Use DI

[?]

Unit of Use DI Number: 10197344099023 CLOSE

Direct Marking (DM)

[?]

Device Subject to Direct Marking (DM), but Excepted: No
DM DI Different from Primary DI: No
DM DI Number: None
CLOSE

Production Identifier(s) in UDI

[?]

Lot or Batch Number: Yes
Serial Number: No
Expiration Date: No
Manufacturing Date: Yes
Donation Identification Number: No CLOSE

Customer Contact

[?]

Phone: +1(800)633-5463
Email: service@medline.com

MENU
- Home
- About
- News
- API
- Download
- Help

FDA TOOLS & RESOURCES