AccessGUDID - DEVICE: IHN (00860011457800)

GUDID

Device Identifier (DI) Information

Brand Name: IHN
Version or Model: 40015
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: IHN, Inc.

Primary DI Number: 00860011457800
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 183692342 *Terms of Use

Device Description: 3x10=0 Full Extension Knee Device

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):	Yes
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?
63464	Lower limb sliding exerciser, non-powered	A non-powered device intended to encourage active movement of a patient’s lower limb(s) by assisting linear (or circular) movement of the foot, by flexion/extension at the knee, for rehabilitation and/or to help prevent deep vein thrombosis. It can be in the form of pad worn on the heel for sliding on a floor (or other smooth surface), or a frame with a moveable section placed on a bed. This is a reusable device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
HST	Apparatus, Traction, Non-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: 125ff3e7-419e-4375-b67b-a0ec3c6de609
Public Version Date: February 15, 2024
Public Version Number: 1
DI Record Publish Date: February 07, 2024

Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]

Package DI Number	Quantity per Package	Contains DI Package	Package Discontinue Date	Package Status	Package Type
10860011457807	2	00860011457800		In Commercial Distribution	Box
20860011457804	16	00860011457800		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: No
Manufacturing Date: Yes
Donation Identification Number: No CLOSE

Customer Contact

[?]

Phone: +1 517-706-0060
Email: info@straightknee.com

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

FDA TOOLS & RESOURCES