Wullstein retractor 10-420-13

GUDID 04250676729484

3:3 prongs, semi-sharp, dismountable 13.5 cm

Spiggle & Theis Medizintechnik GmbH

Hand-held surgical retractor, reusable

• Primary Device ID: 04250676729484
• NIH Device Record Key: 72902387-a764-47b8-aa60-b536e60320e3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Wullstein retractor
• Version Model Number: 10-420-13
• Catalog Number: 10-420-13
• 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	04250676729484 [Primary]

FDA Product Code

• GAD: RETRACTOR

Sterilization

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

[04250676729484]

Moist Heat or Steam Sterilization

[04250676729484]

Moist Heat or Steam Sterilization

[04250676729484]

Moist Heat or Steam Sterilization

[04250676729484]

Moist Heat or Steam Sterilization

[04250676729484]

Moist Heat or Steam Sterilization

[04250676729484]

Moist Heat or Steam Sterilization

[04250676729484]

Moist Heat or Steam Sterilization

[04250676729484]

Moist Heat or Steam Sterilization

[04250676729484]

Moist Heat or Steam Sterilization

[04250676729484]

Moist Heat or Steam Sterilization

[04250676729484]

Moist Heat or Steam Sterilization

[04250676729484]

Moist Heat or Steam Sterilization

[04250676729484]

Moist Heat or Steam Sterilization

[04250676729484]

Moist Heat or Steam Sterilization

[04250676729484]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-09-19
• Device Publish Date: 2022-09-09

On-Brand Devices [Wullstein retractor]

• 04250676729545: 3:3 prongs, semi-sharp, dismountable 11 cm
• 04250676729538: 3:3 prongs, semi-sharp, dismountable 16 cm
• 04250676729484: 3:3 prongs, semi-sharp, dismountable 13.5 cm
• 04250676729965: 3:3 prongs, semi-sharp 16 cm
• 04250676729804: 3:3 prongs, semi-sharp 11 cm
• 04250676729637: 3:3 prongs, semi-sharp 13.5 cm
• 04250676729941: black coated, 3:3 prongs, semi-sharp 11.5 cm