CASPAR LUMBAR SPECULA 416-823

GUDID 00192896096363

CASPAR LUMBAR SPECULA BLACK ANODIZED COATED

SONTEC INSTRUMENTS, INC.

Bone lever/elevator Bone lever/elevator Bone lever/elevator Bone lever/elevator Bone lever/elevator Bone lever/elevator Bone lever/elevator Bone lever/elevator Bone lever/elevator Bone lever/elevator Bone lever/elevator Bone lever/elevator Bone lever/elevator Bone lever/elevator, reusable Bone lever/elevator, reusable Bone lever/elevator, reusable Bone lever/elevator, reusable Bone lever/elevator, reusable Bone lever/elevator, reusable Bone lever/elevator, reusable

• Primary Device ID: 00192896096363
• NIH Device Record Key: 9b2ed8ee-3e9c-456e-bb03-e11d3c704f58
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CASPAR LUMBAR SPECULA
• Version Model Number: 416-823
• Catalog Number: 416-823
• 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: 800-821-7496
• Email: info@sontecinstruments.com
• Phone: 800-821-7496
• Email: info@sontecinstruments.com
• Phone: 800-821-7496
• Email: info@sontecinstruments.com
• Phone: 800-821-7496
• Email: info@sontecinstruments.com
• Phone: 800-821-7496
• Email: info@sontecinstruments.com
• Phone: 800-821-7496
• Email: info@sontecinstruments.com
• Phone: 800-821-7496
• Email: info@sontecinstruments.com
• Phone: 800-821-7496
• Email: info@sontecinstruments.com
• Phone: 800-821-7496
• Email: info@sontecinstruments.com
• Phone: 800-821-7496
• Email: info@sontecinstruments.com
• Phone: 800-821-7496
• Email: info@sontecinstruments.com
• Phone: 800-821-7496
• Email: info@sontecinstruments.com
• Phone: 800-821-7496
• Email: info@sontecinstruments.com
• Phone: 800-821-7496
• Email: info@sontecinstruments.com
• Phone: 800-821-7496
• Email: info@sontecinstruments.com
• Phone: 800-821-7496
• Email: info@sontecinstruments.com
• Phone: 800-821-7496
• Email: info@sontecinstruments.com
• Phone: 800-821-7496
• Email: info@sontecinstruments.com
• Phone: 800-821-7496
• Email: info@sontecinstruments.com
• Phone: 800-821-7496
• Email: info@sontecinstruments.com

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896096363 [Primary]

FDA Product Code

• FXE: Speculum, Non-Illuminated

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[00192896096363]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896096363]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896096363]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896096363]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896096363]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896096363]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896096363]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896096363]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896096363]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896096363]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896096363]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896096363]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896096363]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896096363]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896096363]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896096363]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896096363]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896096363]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896096363]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-05-17
• Device Publish Date: 2019-05-09

On-Brand Devices [CASPAR LUMBAR SPECULA]

• 00192896079441: CASPAR LUMBAR SPECULA NON-REFLECTIVE BLACK ANNODIZED COATED
• 00192896079434: CASPAR LUMBAR SPECULA NON-REFLECTIVE BLACK ANNODIZED COATED
• 00192896079427: CASPAR LUMBAR SPECULA NON-REFLECTIVE BLACK ANNODIZED COATED
• 00192896079410: CASPAR LUMBAR SPECULA NON-REFLECTIVE BLACK ANNODIZED COATED
• 00192896079403: CASPAR LUMBAR SPECULA NON-REFLECTIVE BLACK ANNODIZED COATED
• 00192896096363: CASPAR LUMBAR SPECULA BLACK ANODIZED COATED