AccessGUDID - DEVICE: Powerline Acessory (00817463027136)

GUDID

Device Identifier (DI) Information

Brand Name: Powerline Acessory
Version or Model: 44677
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: OAKWORKS, INC.

Primary DI Number: 00817463027136
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 130256837 *Terms of Use

Device Description: 27" Powerline Table Extender

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):	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?
66492	Radiology table extension	A non-powered attachment to a radiology table intended to increase (lengthen) the area of flat tabletop for patient adaptation/examination (e.g., to accommodate a tall patient or to replace a contoured headrest during neck examination); it is not primarily intended for interventional procedures/surgery. It is a flat padded device with tabletop connection rods; it is not a dedicated foot or head rest.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
LGX	Table, Examination, Medical, Powered

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: 21d1c7ab-8e0b-4241-a4b4-62805e6aa123
Public Version Date: January 09, 2025
Public Version Number: 2
DI Record Publish Date: December 06, 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: Yes
Expiration Date: No
Manufacturing Date: Yes
Donation Identification Number: No CLOSE

Customer Contact

[?]

No Customer Contact currently defined

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