Schnidt tonsil forceps 40-451-19

GUDID 04250676730756

one ring open, slender strongly curved, 19 cm

Spiggle & Theis Medizintechnik GmbH

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

• Primary Device ID: 04250676730756
• NIH Device Record Key: 834211ca-d2e0-4a2c-8a20-2b04526285c9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Schnidt tonsil forceps
• Version Model Number: 40-451-19
• Catalog Number: 40-451-19
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	04250676730756 [Primary]

FDA Product Code

• LRC: INSTRUMENT, ENT MANUAL SURGICAL

Sterilization

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

[04250676730756]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-11-19
• Device Publish Date: 2024-11-11

On-Brand Devices [Schnidt tonsil forceps]

• 04250676730572: one ring open, slender slightly curved, 19 cm
• 04250676730756: one ring open, slender strongly curved, 19 cm