AccessGUDID - DEVICE: Veeda (00810462020412)

GUDID

Device Identifier (DI) Information

Brand Name: Veeda
Version or Model: VPRW14US
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: NATURALENA BRANDS INC.

Primary DI Number: 00810462020412
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 14
Labeler D-U-N-S® Number*: 047756618 *Terms of Use

Device Description: Veeda Natural Cotton Ultra-Thin Day Pads with Wings, 14 ct

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:	Yes
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?
40545	Menstrual pad, unscented	A non-deodorized, feminine hygiene product (a pad) that is held in place externally to absorb menstrual or other vaginal discharge. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
HHD	Pad, Menstrual, Unscented

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: c5aaa154-9914-4991-9182-b00cd743ffc1
Public Version Date: May 23, 2019
Public Version Number: 2
DI Record Publish Date: September 25, 2018

Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]

Package DI Number	Quantity per Package	Contains DI Package	Package Status	Package Type
00810462021280	3	00810462020412	In Commercial Distribution	inner case
40810462020410	12	00810462020412	In Commercial Distribution	case
30810462020413	24	00810462020412	In Commercial Distribution	case
00810462021396	6	00810462020412	In Commercial Distribution	case
10810462021287	8	00810462021280	In Commercial Distribution	case

Secondary DI

[?]

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

Unit of Use DI

[?]

Unit of Use DI Number: 00810462022614 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

[?]

No Customer Contact currently defined

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