AccessGUDID - DEVICE: Drive (00822383511863)

GUDID

Device Identifier (DI) Information

Brand Name: Drive
Version or Model: PL-STDS4Y4706
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: Drive Devilbiss Healthcare

Primary DI Number: 00822383511863
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 867673159 *Terms of Use

Device Description: ViperGT,20"Recl,FlpBackRemFull,1/ea

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?
57978	Wheelchair recliner, battery-powered	A battery-powered mobile device designed to tilt (recline) a standard type wheelchair and occupant (not bariatric) to enable healthcare providers give treatment at a degree of tilt most efficient for them. The device includes a platform onto which the wheelchair/occupant is reversed and secured, and rechargeable batteries that drive an electric motor to power the tilting mechanism. It may include additional back- and headrest and may be moved on wheels for repositioning within a room or facility. It is used for treatments in dentistry, ophthalmology, maxillofacial and ear/nose/throat (ENT), podiatry (including diabetic foot care), physical therapy, and personal care.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
IOR	Wheelchair, mechanical

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
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 88ac4df4-72d2-4642-aed1-7bfef26081c8
Public Version Date: March 29, 2018
Public Version Number: 2
DI Record Publish Date: July 10, 2017

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

[?]

No Customer Contact currently defined

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