Fisch footplate perforator 10-658-07

GUDID 04250676735539

0.7 mm, 16 cm

Spiggle & Theis Medizintechnik GmbH

Automatic cranial perforator, reusable

• Primary Device ID: 04250676735539
• NIH Device Record Key: c763e606-c0d6-4bc2-abce-6758665626d2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Fisch footplate perforator
• Version Model Number: 10-658-07
• Catalog Number: 10-658-07
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	04250676735539 [Primary]

FDA Product Code

• JYS: PERFORATOR, EAR-LOBE

Sterilization

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

[04250676735539]

Moist Heat or Steam Sterilization

[04250676735539]

Moist Heat or Steam Sterilization

[04250676735539]

Moist Heat or Steam Sterilization

[04250676735539]

Moist Heat or Steam Sterilization

[04250676735539]

Moist Heat or Steam Sterilization

[04250676735539]

Moist Heat or Steam Sterilization

[04250676735539]

Moist Heat or Steam Sterilization

[04250676735539]

Moist Heat or Steam Sterilization

[04250676735539]

Moist Heat or Steam Sterilization

[04250676735539]

Moist Heat or Steam Sterilization

[04250676735539]

Moist Heat or Steam Sterilization

[04250676735539]

Moist Heat or Steam Sterilization

[04250676735539]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-09-07
• Device Publish Date: 2023-08-30

On-Brand Devices [Fisch footplate perforator]

• 04250381849538: 0.8 mm, 16 cm
• 04250381849514: 0.6 mm, 16 cm
• 04250381849507: 0.5 mm, 16 cm
• 04250381849491: 0.4 mm, 16 cm
• 04250381848449: 0.3 mm, 16 cm
• 04250676735539: 0.7 mm, 16 cm