Jackson laryngoscope 50-232-03

GUDID 04250676739988

size 3, handle removable, light carrier satin finished inside, 180 mm long

Spiggle & Theis Medizintechnik GmbH

Rigid intubation laryngoscope, reusable

• Primary Device ID: 04250676739988
• NIH Device Record Key: 3f770072-df4c-438f-a193-8c0ddc4c0330
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Jackson laryngoscope
• Version Model Number: 50-232-03
• Catalog Number: 50-232-03
• Company DUNS: 332893028
• Company Name: Spiggle & Theis Medizintechnik GmbH
• 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: true
• 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: +492206908165
• Email: c.winterschladen@spiggle-theis.com
• Phone: +492206908165
• Email: c.winterschladen@spiggle-theis.com
• Phone: +492206908165
• Email: c.winterschladen@spiggle-theis.com
• Phone: +492206908165
• Email: c.winterschladen@spiggle-theis.com
• Phone: +492206908165
• Email: c.winterschladen@spiggle-theis.com
• Phone: +492206908165
• Email: c.winterschladen@spiggle-theis.com
• Phone: +492206908165
• Email: c.winterschladen@spiggle-theis.com
• Phone: +492206908165
• Email: c.winterschladen@spiggle-theis.com
• Phone: +492206908165
• Email: c.winterschladen@spiggle-theis.com
• Phone: +492206908165
• Email: c.winterschladen@spiggle-theis.com
• Phone: +492206908165
• Email: c.winterschladen@spiggle-theis.com
• Phone: +492206908165
• Email: c.winterschladen@spiggle-theis.com
• Phone: +492206908165
• Email: c.winterschladen@spiggle-theis.com
• Phone: +492206908165
• Email: c.winterschladen@spiggle-theis.com
• Phone: +492206908165
• Email: c.winterschladen@spiggle-theis.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	04250676739988 [Primary]

FDA Product Code

• CCW: LARYNGOSCOPE, RIGID

Sterilization

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

[04250676739988]

Moist Heat or Steam Sterilization

[04250676739988]

Moist Heat or Steam Sterilization

[04250676739988]

Moist Heat or Steam Sterilization

[04250676739988]

Moist Heat or Steam Sterilization

[04250676739988]

Moist Heat or Steam Sterilization

[04250676739988]

Moist Heat or Steam Sterilization

[04250676739988]

Moist Heat or Steam Sterilization

[04250676739988]

Moist Heat or Steam Sterilization

[04250676739988]

Moist Heat or Steam Sterilization

[04250676739988]

Moist Heat or Steam Sterilization

[04250676739988]

Moist Heat or Steam Sterilization

[04250676739988]

Moist Heat or Steam Sterilization

[04250676739988]

Moist Heat or Steam Sterilization

[04250676739988]

Moist Heat or Steam Sterilization

[04250676739988]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-01-07
• Device Publish Date: 2024-12-30

On-Brand Devices [Jackson laryngoscope]

• 04250676739971: size 2, handle removable, light carrier satin finished inside, 171 mm long
• 04250676739988: size 3, handle removable, light carrier satin finished inside, 180 mm long