Tablet dish 80-512-00

GUDID 04250381892039

stainless steel Ø 65 mm, height 19 mm

Spiggle & Theis Medizintechnik GmbH

General-purpose bowl, reusable

• Primary Device ID: 04250381892039
• NIH Device Record Key: 21b02506-c11f-4a00-9fb1-c42a6d6bc267
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Tablet dish
• Version Model Number: 80-512-00
• Catalog Number: 80-512-00
• 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
• Phone: +492206908165
• Email: c.winterschladen@spiggle-theis.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	04250381892039 [Primary]

FDA Product Code

• LRC: INSTRUMENT, ENT MANUAL SURGICAL

Sterilization

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

[04250381892039]

Moist Heat or Steam Sterilization

[04250381892039]

Moist Heat or Steam Sterilization

[04250381892039]

Moist Heat or Steam Sterilization

[04250381892039]

Moist Heat or Steam Sterilization

[04250381892039]

Moist Heat or Steam Sterilization

[04250381892039]

Moist Heat or Steam Sterilization

[04250381892039]

Moist Heat or Steam Sterilization

[04250381892039]

Moist Heat or Steam Sterilization

[04250381892039]

Moist Heat or Steam Sterilization

[04250381892039]

Moist Heat or Steam Sterilization

[04250381892039]

Moist Heat or Steam Sterilization

[04250381892039]

Moist Heat or Steam Sterilization

[04250381892039]

Moist Heat or Steam Sterilization

[04250381892039]

Moist Heat or Steam Sterilization

[04250381892039]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-06-02
• Device Publish Date: 2025-05-23

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• 04250676744425 - Negus tonsil forceps: 2025-08-07 slender, wide curve 19 cm
• 04250676744432 - Negus tonsil forceps: 2025-08-07 slender, narrow curve 19 cm
• 04250676744449 - Overholt-Geissdoerfer tonsil forceps: 2025-08-07 curved 21 cm
• 04250676744456 - Mikulicz tonsil forceps: 2025-08-07 curved, 1:2 teeth 18 cm
• 04250676744463 - Halsted-Mosquito artery forceps: 2025-08-07 straight, anatomical 12.5 cm