AccessGUDID - DEVICE: Arthrex® (00888867020009)

GUDID

Device Identifier (DI) Information

Brand Name: Arthrex®
Version or Model: AR-1606SV
Commercial Distribution Status: In Commercial Distribution
Catalog Number: AR-1606SV
Company Name: ARTHREX, INC.

Primary DI Number: 00888867020009
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 131747628 *Terms of Use

Device Description: STAR SLEEVE, SMALL, VELCRO

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:	Yes
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?
35714	Orthopaedic casting stand	A structure/frame designed to hold and support a patient's torso or limb (arm or leg) in an appropriate position during an orthopaedic casting procedure. It typically consists of an adjustable base/pedestal and frame with a set of detachable components including limb-positioning attachments to maintain optimum joint alignment, supports for resting limbs, and blades for forming the cast. Typically the body part is placed on a blade and the cast material is wrapped around it; after completing the cast, the blade is removed from the cast to provide space for improved blood circulation and patient comfort. This is a reusable device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
KQZ	COMPONENT, TRACTION, NON-INVASIVE

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: Yes
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: dd0ccde7-a9e3-4ddb-8cd8-dcb62ee41e7d
Public Version Date: August 05, 2019
Public Version Number: 2
DI Record Publish Date: August 03, 2018

Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]

Package DI Number	Quantity per Package	Contains DI Package	Package Discontinue Date	Package Status	Package Type
10888867020006	6	00888867020009		In Commercial Distribution	Box

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

Customer Contact

[?]

Phone: +1(800)934-4404
Email: complaints@arthrex.com

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