SUTURE INSTRUMENT

GUDID 04049047087892

SUTURE INSTRUMENT FOR SUBCUTANEOUS FASCIAL CLOSURE,Ø2.3 MM WORKING LENGTH 140 MM

Gimmi GmbH

Suturing unit, reusable

• Primary Device ID: 04049047087892
• NIH Device Record Key: dead26db-9723-47de-89c3-182749c0e5ea
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SUTURE INSTRUMENT
• Version Model Number: S.0904.07
• Company DUNS: 316152610
• Company Name: Gimmi GmbH
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +497461965900
• Email: contact@gimmi.de
• Phone: +497461965900
• Email: contact@gimmi.de
• Phone: +497461965900
• Email: contact@gimmi.de
• Phone: +497461965900
• Email: contact@gimmi.de
• Phone: +497461965900
• Email: contact@gimmi.de
• Phone: +497461965900
• Email: contact@gimmi.de
• Phone: +497461965900
• Email: contact@gimmi.de
• Phone: +497461965900
• Email: contact@gimmi.de
• Phone: +497461965900
• Email: contact@gimmi.de
• Phone: +497461965900
• Email: contact@gimmi.de
• Phone: +497461965900
• Email: contact@gimmi.de
• Phone: +497461965900
• Email: contact@gimmi.de
• Phone: +497461965900
• Email: contact@gimmi.de
• Phone: +497461965900
• Email: contact@gimmi.de
• Phone: +497461965900
• Email: contact@gimmi.de
• Phone: +497461965900
• Email: contact@gimmi.de
• Phone: +497461965900
• Email: contact@gimmi.de

Device Identifiers

Device Issuing Agency	Device ID
GS1	04049047087892 [Primary]

FDA Product Code

• GCJ: Laparoscope, General & Plastic Surgery

Sterilization

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

[04049047087892]

Moist Heat or Steam Sterilization

[04049047087892]

Moist Heat or Steam Sterilization

[04049047087892]

Moist Heat or Steam Sterilization

[04049047087892]

Moist Heat or Steam Sterilization

[04049047087892]

Moist Heat or Steam Sterilization

[04049047087892]

Moist Heat or Steam Sterilization

[04049047087892]

Moist Heat or Steam Sterilization

[04049047087892]

Moist Heat or Steam Sterilization

[04049047087892]

Moist Heat or Steam Sterilization

[04049047087892]

Moist Heat or Steam Sterilization

[04049047087892]

Moist Heat or Steam Sterilization

[04049047087892]

Moist Heat or Steam Sterilization

[04049047087892]

Moist Heat or Steam Sterilization

[04049047087892]

Moist Heat or Steam Sterilization

[04049047087892]

Moist Heat or Steam Sterilization

[04049047087892]

Moist Heat or Steam Sterilization

[04049047087892]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-08-01
• Device Publish Date: 2024-07-24

Devices Manufactured by Gimmi GmbH

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• 04049047075295 - Gimmi: 2025-05-29 HARTMANN EAR SPECULA FIG. 1, STAINLESS STEEL Ø 3.0 MM
• 04049047075301 - Gimmi: 2025-05-29 HARTMANN EAR SPECULA FIG. 2, STAINLESS STEEL Ø 3.5 MM
• 04049047075318 - Gimmi: 2025-05-29 HARTMANN EAR SPECULA FIG. 3, STAINLESS STEEL Ø 4.5 MM
• 04049047075325 - Gimmi: 2025-05-29 HARTMANN EAR SPECULA FIG. 4, STAINLESS STEEL Ø 5.5 MM
• 04049047075332 - Gimmi: 2025-05-29 HARTMANN EAR SPECULA FIG. 5, STAINLESS STEEL Ø 6.0 MM
• 04049047075417 - Gimmi: 2025-05-29 HARTMANN EAR SPECULA FIG. 1, BRASS BLACK CHROMED Ø 2.0 MM
• 04049047075424 - Gimmi: 2025-05-29 HARTMANN EAR SPECULA FIG. 2, BRASS BLACK CHROMED Ø 3.5 MM