Ochsner-Kocher artery forceps 40-650-39

GUDID 04250676744753

straight, 1:2 teeth 20 cm

Spiggle & Theis Medizintechnik GmbH

Surgical soft-tissue manipulation forceps, alligator, reusable

• Primary Device ID: 04250676744753
• NIH Device Record Key: 60bab4f4-ba13-4776-a44b-65286d898592
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Ochsner-Kocher artery forceps
• Version Model Number: 40-650-39
• Catalog Number: 40-650-39
• 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	04250676744753 [Primary]

FDA Product Code

• KAE: FORCEPS, ENT

Sterilization

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

[04250676744753]

Moist Heat or Steam Sterilization

[04250676744753]

Moist Heat or Steam Sterilization

[04250676744753]

Moist Heat or Steam Sterilization

[04250676744753]

Moist Heat or Steam Sterilization

[04250676744753]

Moist Heat or Steam Sterilization

[04250676744753]

Moist Heat or Steam Sterilization

[04250676744753]

Moist Heat or Steam Sterilization

[04250676744753]

Moist Heat or Steam Sterilization

[04250676744753]

Moist Heat or Steam Sterilization

[04250676744753]

Moist Heat or Steam Sterilization

[04250676744753]

Moist Heat or Steam Sterilization

[04250676744753]

Moist Heat or Steam Sterilization

[04250676744753]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-08-07
• Device Publish Date: 2025-07-30

On-Brand Devices [Ochsner-Kocher artery forceps]

• 04250676733078: curved, 1:2 teeth 20 cm
• 04250676733061: curved, 1:2 teeth 18.5 cm
• 04250676733054: straight, 1:2 teeth 20 cm
• 04250676733047: straight, 1:2 teeth 18.5 cm
• 04250676744777: curved, 1:2 teeth 20 cm
• 04250676744760: curved, 1:2 teeth 18 cm
• 04250676744753: straight, 1:2 teeth 20 cm
• 04250676744746: straight, 1:2 teeth 18 cm