AccessGUDID - DEVICE: Pure&Clean (00852421007614)

GUDID

Device Identifier (DI) Information

Brand Name: Pure&Clean
Version or Model: 08.2019
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 1WCQ-RXP
Company Name: Pure & Clean, LLC

Primary DI Number: 00852421007614
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 045315650 *Terms of Use

Device Description: Wound Solutions Rx Wound Pour Cap Quart

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):	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?
37207	Surgical/medical procedure irrigation fluid	A solution, typically saline, intended to be used to flush an anatomical site for clearing and cleaning during a surgical/medical procedure (e.g., ocular area during eye surgery, middle ear during an ENT procedure). The solution may be supplied in a prefilled syringe. After application, this device cannot be reused.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
FRO	Dressing, Wound, Drug

FDA Premarket Submission

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

Device Exempt from Premarket Submission: No 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
Storage Environment Temperature: more than 32 Degrees Fahrenheit
Storage Environment Temperature: more than 0 Degrees Celsius

Clinically Relevant Size

[?]

Size Type Text
Total Volume: 32 Fluid Ounce

Device Record Status

Public Device Record Key: 8225a34b-8460-4a40-a1e1-17e88b8b83f6
Public Version Date: August 14, 2023
Public Version Number: 1
DI Record Publish Date: August 04, 2023

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: No
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: No
Donation Identification Number: No CLOSE

Customer Contact

[?]

Phone: 417-725-3787
Email: info@pureandclean.us

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

FDA TOOLS & RESOURCES