Kocher artery forceps 40-650-27

GUDID 04250676744630

straight, 1:2 teeth, fine 16 cm

Spiggle & Theis Medizintechnik GmbH

Surgical soft-tissue manipulation forceps, alligator, reusable

• Primary Device ID: 04250676744630
• NIH Device Record Key: 5c42ffa2-54a0-4e1c-8659-f6b5517f70b6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Kocher artery forceps
• Version Model Number: 40-650-27
• Catalog Number: 40-650-27
• 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	04250676744630 [Primary]

FDA Product Code

• KAE: FORCEPS, ENT

Sterilization

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

[04250676744630]

Moist Heat or Steam Sterilization

[04250676744630]

Moist Heat or Steam Sterilization

[04250676744630]

Moist Heat or Steam Sterilization

[04250676744630]

Moist Heat or Steam Sterilization

[04250676744630]

Moist Heat or Steam Sterilization

[04250676744630]

Moist Heat or Steam Sterilization

[04250676744630]

Moist Heat or Steam Sterilization

[04250676744630]

Moist Heat or Steam Sterilization

[04250676744630]

Moist Heat or Steam Sterilization

[04250676744630]

Moist Heat or Steam Sterilization

[04250676744630]

Moist Heat or Steam Sterilization

[04250676744630]

Moist Heat or Steam Sterilization

[04250676744630]

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 [Kocher artery forceps]

• 04250676732941: curved, 1:2 teeth, fine 16 cm
• 04250676732934: curved, 1:2 teeth, fine 14 cm
• 04250676732927: straight, 1:2 teeth, fine 16 cm
• 04250676732910: straight, 1:2 teeth, fine 14 cm
• 04250676744654: curved, 1:2 teeth, fine 16 cm
• 04250676744647: curved, 1:2 teeth, fine 14 cm
• 04250676744630: straight, 1:2 teeth, fine 16 cm
• 04250676744623: straight, 1:2 teeth, fine 14 cm