FDA.report

NA

Primary DI
00840085246128
Brand
NA
Company
HYHTE HOLDINGS, INC.
Model
KZF090000
Catalog number
KZF090000
Device description
SPACER DISASSEMBLY TOOL
Published
2022-05-11
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
false
Single use
true

Related Records

Contact Domains

Product Codes

CodeName
OVDIntervertebral Fusion Device With Integrated Fixation, Lumbar

Product Code Classifications

CodeDeviceSpecialtyClass
OVDIntervertebral Fusion Device With Integrated Fixation, LumbarOrthopedic2

Identifiers And Packaging

IdentifierTypeAgencyPackage quantityStatus
00840085246128PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifierGTIN-14 normalizedUPC-AEAN-13
00840085246128008400852461288400852461280840085246128

GMDN Terms

TermDefinition
Callous file/rasp, reusableA hand-held manual instrument with a surface(s) of coarse and/or fine grooves or teeth at the distal working end designed to be rubbed back and forth over the skin to remove callouses (i.e., hardened and thickened protrusions of skin commonly known as hard skin). This is a reusable device.

Sterilization Methods

Method
Moist Heat or Steam Sterilization

Contacts

PhoneEmail
7608148047PARKER@ASTURAMEDICAL.COM

Regulatory Flags

DUNS number
073029645
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
false
Expiration date on label
false
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
true

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