AccessGUDID - DEVICE: Adaptive Desk (00850001752428)

GUDID

Device Identifier (DI) Information

Brand Name: Adaptive Desk
Version or Model: R250
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: RIFTON EQUIPMENT

Primary DI Number: 00850001752428
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 808251438 *Terms of Use

Device Description: Adaptive classroom desk

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":	Yes
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?
31219	Ergonomic workdesk, manual	A manually-operated desk designed with ergonomic adjustments to provide improved personal work-position flexibility and to help prevent/reduce physical problems associated with sedentary work. It is intended to be used for work or training typically by patients with back problems or disabilities. It typically includes a mechanical height-adjustable worktop and may include tilting-functions or raised table edges; it is typically used for computer and writing work in an office, school, or home setting.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
INW	Table, Mechanical

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: a9ac9a61-853a-49c1-adc6-2b5c0bcd5870
Public Version Date: February 12, 2025
Public Version Number: 1
DI Record Publish Date: February 04, 2025

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: 800-571-8198
Email: sales@rifton.com

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