AccessGUDID - DEVICE: Walgreens (00311917158891)

GUDID

Device Identifier (DI) Information

Brand Name: Walgreens
Version or Model: 276737
Commercial Distribution Status: In Commercial Distribution
Catalog Number: WRX276737V1
Company Name: WALGREEN CO.

Primary DI Number: 00311917158891
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 008965063 *Terms of Use

Device Description: Transfer Bench. Supports up to 300 lbs (136 kg).

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):	Yes
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	No
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?
41051	Bath board	A device in the form of a flat board designed to be sat upon by an adult patient who is bathing in a bath (usually while being attended/assisted) to elevate the patient out of the water except for the feet. The patient is typically disabled, infirm, or undergoing medical treatment and cannot sit normally in a bath. The device typically includes a solid or ribbed flat seat and is secured across the rim of the bath; it is typically made of water-resistant or waterproof materials. The device may be used in a hospital, institution, or home.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
ILS	Adaptor, Hygiene

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: 50d8d536-8358-46b3-bb89-8f83f9ffde79
Public Version Date: July 22, 2020
Public Version Number: 1
DI Record Publish Date: July 14, 2020

Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]

Package DI Number	Quantity per Package	Contains DI Package	Package Discontinue Date	Package Status	Package Type
10311917158898	2	00311917158891		In Commercial Distribution	Case

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: Yes
Serial Number: No
Expiration Date: No
Manufacturing Date: No
Donation Identification Number: No CLOSE

Customer Contact

[?]

Phone: 1-800-925-4733
Email: consumerrelations.pq@walgreens.com

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