AccessGUDID - DEVICE: TRANSFER BOARD SUPPORT ROD (10841736112707)

GUDID

Device Identifier (DI) Information

Brand Name: TRANSFER BOARD SUPPORT ROD
Version or Model: 4-030-22-2
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: SKYTRON LLC

Primary DI Number: 10841736112707
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 078375583 *Terms of Use

Device Description: TRANSFER BOARD SUPPORT ROD 5/8 3600B/6700B TABLES

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?
62758	Medical table top floor stand, non-powered	A non-powered device designed to support and stabilize from the floor a medical table top [e.g., an operating table top for hand surgery, or a table top for cardiopulmonary resuscitation (CPR)] or table [e.g., base of a traction table]. It may be in the form of a slender vertical telescopic post, a framework or a multi-jointed structure, and is typically used for support of cantilevered table tops or extensions; it is not intended to function as the primary support for the main body of an operating table top (i.e., not an operating table base).	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
LWG	Surgical Table Cushion

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: 5e210914-fa87-4bf5-a64c-0a1c445e9d7c
Public Version Date: January 20, 2025
Public Version Number: 3
DI Record Publish Date: October 15, 2019

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: 800-759-8766
Email: info@skytron.us

MENU
- Home
- About
- News
- API
- Download
- Help

FDA TOOLS & RESOURCES