AccessGUDID - DEVICE: C-MATT (00815073025283)

GUDID

Device Identifier (DI) Information

Brand Name: C-MATT
Version or Model: H10849
Commercial Distribution Status: In Commercial Distribution
Catalog Number: H10849
Company Name: CASCO MANUFACTURING SOLUTIONS, INC.

Primary DI Number: 00815073025283
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 004253936 *Terms of Use

Device Description: Stretcher Mat Cover Only Conductive 2 Tapers 4 x 31 x 76

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":	No
For Single-Use:	No
Prescription Use (Rx):	No
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?
35180	Conductive bed mattress cover	A device made of soft, conductive material that is shaped to fit over a bed mattress to create a physical barrier to protect the mattress, prevent cross-contamination and the build-up of static electricity. This is a single-patient device that is used for a limited time, without laundering, until considered inappropriate for further use and then discarded (e.g., incinerated).	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
FMW	COVER, MATTRESS (MEDICAL PURPOSES)

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: dc7d9315-9bac-4aa8-a8fd-9ec02d1ab282
Public Version Date: April 15, 2019
Public Version Number: 1
DI Record Publish Date: April 05, 2019

Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]

Package DI Number	Quantity per Package	Contains DI Package	Package Discontinue Date	Package Status	Package Type
No Package DIs found

Secondary DI

[?]

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

Unit of Use DI

[?]

Unit of Use DI Number: No Unit of Use DI Numbers Found CLOSE

Direct Marking (DM)

[?]

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

Production Identifier(s) in UDI

[?]

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

Customer Contact

[?]

No Customer Contact currently defined

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