forceps 15-504-08

GUDID 04250676728517

angled, very fine 11.5 mm, length 8.5 cm

Spiggle & Theis Medizintechnik GmbH

Surgical soft-tissue manipulation forceps, tweezers-like, reusable

• Primary Device ID: 04250676728517
• NIH Device Record Key: 3c076604-9663-4b92-b951-11af7269cfea
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: forceps
• Version Model Number: 15-504-08
• Catalog Number: 15-504-08
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	04250676728517 [Primary]

FDA Product Code

• KAE: FORCEPS, ENT

Sterilization

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

[04250676728517]

Moist Heat or Steam Sterilization

[04250676728517]

Moist Heat or Steam Sterilization

[04250676728517]

Moist Heat or Steam Sterilization

[04250676728517]

Moist Heat or Steam Sterilization

[04250676728517]

Moist Heat or Steam Sterilization

[04250676728517]

Moist Heat or Steam Sterilization

[04250676728517]

Moist Heat or Steam Sterilization

[04250676728517]

Moist Heat or Steam Sterilization

[04250676728517]

Moist Heat or Steam Sterilization

[04250676728517]

Moist Heat or Steam Sterilization

[04250676728517]

Moist Heat or Steam Sterilization

[04250676728517]

Moist Heat or Steam Sterilization

[04250676728517]

Moist Heat or Steam Sterilization

[04250676728517]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-10-03
• Device Publish Date: 2025-09-25

On-Brand Devices [forceps]

• 04250676714770: 1:2 teeth, small 18 cm
• 04250676738295: 3:4 teeth 14.5 cm
• 04250676738288: 1:2 teeth 18 cm
• 04250676728517: angled, very fine 11.5 mm, length 8.5 cm