Fiberglass light carrier 50-234-02

GUDID 04250676736048

for Jackson laryngoscope 50-233-02 & 50-232-02

Spiggle & Theis Medizintechnik GmbH

Fibreoptic light cable

• Primary Device ID: 04250676736048
• NIH Device Record Key: 49920519-3461-4767-899b-feaaca701e04
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Fiberglass light carrier
• Version Model Number: 50-234-02
• Catalog Number: 50-234-02
• 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	04250676736048 [Primary]

FDA Product Code

• LRC: INSTRUMENT, ENT MANUAL SURGICAL

Sterilization

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

[04250676736048]

Moist Heat or Steam Sterilization

[04250676736048]

Moist Heat or Steam Sterilization

[04250676736048]

Moist Heat or Steam Sterilization

[04250676736048]

Moist Heat or Steam Sterilization

[04250676736048]

Moist Heat or Steam Sterilization

[04250676736048]

Moist Heat or Steam Sterilization

[04250676736048]

Moist Heat or Steam Sterilization

[04250676736048]

Moist Heat or Steam Sterilization

[04250676736048]

Moist Heat or Steam Sterilization

[04250676736048]

Moist Heat or Steam Sterilization

[04250676736048]

Moist Heat or Steam Sterilization

[04250676736048]

Moist Heat or Steam Sterilization

[04250676736048]

Moist Heat or Steam Sterilization

[04250676736048]

Moist Heat or Steam Sterilization

[04250676736048]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-10-05
• Device Publish Date: 2022-09-27

On-Brand Devices [Fiberglass light carrier]

• 04250676736048: for Jackson laryngoscope 50-233-02 & 50-232-02
• 04250676736017: for Holinger laryngoscope 50-230-02 & 50-229-02
• 04250676736055: for Jackson laryngoscope 50-233-03 & 50-232-03
• 04250676736031: for Jackson laryngoscope 50-233-01 & 50-232-01
• 04250676736024: for Holinger laryngoscope 50-230-03 & 50-229-03
• 04250676736000: for Holinger laryngoscope 50-230-01 & 50-229-01