Müller wire closing forceps 10-713-00

GUDID 04250676721068

straight, rounded tip 0.8x3.5 mm, 8 cm

Spiggle & Theis Medizintechnik GmbH

Wire holding/twisting forceps

• Primary Device ID: 04250676721068
• NIH Device Record Key: 41f6eeca-b8e4-409b-be7f-febbd9270daa
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Müller wire closing forceps
• Version Model Number: 10-713-00
• Catalog Number: 10-713-00
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	04250676721068 [Primary]

FDA Product Code

• NNQ: FORCEPS, WIRE CLOSURE, ENT, NON-STERILE

Sterilization

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

[04250676721068]

Moist Heat or Steam Sterilization

[04250676721068]

Moist Heat or Steam Sterilization

[04250676721068]

Moist Heat or Steam Sterilization

[04250676721068]

Moist Heat or Steam Sterilization

[04250676721068]

Moist Heat or Steam Sterilization

[04250676721068]

Moist Heat or Steam Sterilization

[04250676721068]

Moist Heat or Steam Sterilization

[04250676721068]

Moist Heat or Steam Sterilization

[04250676721068]

Moist Heat or Steam Sterilization

[04250676721068]

Moist Heat or Steam Sterilization

[04250676721068]

Moist Heat or Steam Sterilization

[04250676721068]

Moist Heat or Steam Sterilization

[04250676721068]

Moist Heat or Steam Sterilization

[04250676721068]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-09-21
• Device Publish Date: 2022-09-13

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