Gruber Teflon Cutting Block 350-8454

GUDID 00192896120624

Gruber Teflon Cutting Block Without Grid

SONTEC INSTRUMENTS, INC.

Surgical cutting/shaping board, reusable

Primary Device ID	00192896120624
NIH Device Record Key	25323182-c460-4637-89c7-81dad1cab4e1
Commercial Distribution Status	In Commercial Distribution
Brand Name	Gruber Teflon Cutting Block
Version Model Number	350-8454
Catalog Number	350-8454
Company DUNS	040729840
Company Name	SONTEC INSTRUMENTS, INC.
Device Count	1
DM Exempt	false
Pre-market Exempt	true
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	false
Lot Batch	true
Serial Number	false
Manufacturing Date	false
Expiration Date	false
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	true
RX Perscription	true
OTC Over-The-Counter	false

Customer Support Contacts

Phone	+1(800)821-7496
Email	info@sontecinstruments.com
Phone	+1(800)821-7496
Email	info@sontecinstruments.com
Phone	+1(800)821-7496
Email	info@sontecinstruments.com
Phone	+1(800)821-7496
Email	info@sontecinstruments.com
Phone	+1(800)821-7496
Email	info@sontecinstruments.com
Phone	+1(800)821-7496
Email	info@sontecinstruments.com
Phone	+1(800)821-7496
Email	info@sontecinstruments.com
Phone	+1(800)821-7496
Email	info@sontecinstruments.com
Phone	+1(800)821-7496
Email	info@sontecinstruments.com
Phone	+1(800)821-7496
Email	info@sontecinstruments.com
Phone	+1(800)821-7496
Email	info@sontecinstruments.com
Phone	+1(800)821-7496
Email	info@sontecinstruments.com
Phone	+1(800)821-7496
Email	info@sontecinstruments.com
Phone	+1(800)821-7496
Email	info@sontecinstruments.com
Phone	+1(800)821-7496
Email	info@sontecinstruments.com
Phone	+1(800)821-7496
Email	info@sontecinstruments.com

Device Dimensions

Height	10 Millimeter
Width	55 Millimeter
Length	85 Millimeter
Height	10 Millimeter
Width	55 Millimeter
Length	85 Millimeter
Height	10 Millimeter
Width	55 Millimeter
Length	85 Millimeter
Height	10 Millimeter
Width	55 Millimeter
Length	85 Millimeter
Height	10 Millimeter
Width	55 Millimeter
Length	85 Millimeter
Height	10 Millimeter
Width	55 Millimeter
Length	85 Millimeter
Height	10 Millimeter
Width	55 Millimeter
Length	85 Millimeter
Height	10 Millimeter
Width	55 Millimeter
Length	85 Millimeter
Height	10 Millimeter
Width	55 Millimeter
Length	85 Millimeter
Height	10 Millimeter
Width	55 Millimeter
Length	85 Millimeter
Height	10 Millimeter
Width	55 Millimeter
Length	85 Millimeter
Height	10 Millimeter
Width	55 Millimeter
Length	85 Millimeter
Height	10 Millimeter
Width	55 Millimeter
Length	85 Millimeter
Height	10 Millimeter
Width	55 Millimeter
Length	85 Millimeter
Height	10 Millimeter
Width	55 Millimeter
Length	85 Millimeter
Height	10 Millimeter
Width	55 Millimeter
Length	85 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896120624 [Primary]

FDA Product Code

LXH	Orthopedic manual surgical instrument

Sterilization

Steralize Prior To Use	true
Device Is Sterile	false

[00192896120624]

Dry Heat Sterilization

[00192896120624]

Dry Heat Sterilization

[00192896120624]

Dry Heat Sterilization

[00192896120624]

Dry Heat Sterilization

[00192896120624]

Dry Heat Sterilization

[00192896120624]

Dry Heat Sterilization

[00192896120624]

Dry Heat Sterilization

[00192896120624]

Dry Heat Sterilization

[00192896120624]

Dry Heat Sterilization

[00192896120624]

Dry Heat Sterilization

[00192896120624]

Dry Heat Sterilization

[00192896120624]

Dry Heat Sterilization

[00192896120624]

Dry Heat Sterilization

[00192896120624]

Dry Heat Sterilization

[00192896120624]

Dry Heat Sterilization

[00192896120624]

Dry Heat Sterilization

Device Entry Metadata

Public Version Status	New
Device Record Status	Published
Public Version Number	1
Public Version Date	2024-11-04
Device Publish Date	2024-10-25

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