519650 – Coloplast Altis Single Incision Sling System

ALTIS Coloplast Altis Single Incision Sling System — SKU 519650

The Coloplast Altis Single Incision Sling System (SKU 519650) is offered through Class 1 Inventory under the ALTIS brand, manufactured by Coloplast A/S. No exact FDA GUDID record was found for this specific reference number, so we identify it here using catalog-level detail; the manufacturer’s current labeling remains the authoritative source for specifications.

Product Details

The Coloplast Altis® Single Incision Sling System is designed to provide minimally invasive surgical treatment of female stress urinary incontinence. The kit includes a 7.75 cm sling and helical-type introducers for a mini-sling placement approach via the obturator membrane complex. Each system is for single-patient use.

When comparing this item to similar products from other manufacturers, use SKU 519650 and GTIN 05708932467407 to confirm you’re matching the exact configuration your facility needs.

519650 Ordering & Compatibility

For reordering and inventory matching, use the SKU and GTIN shown on this page. FDA records list this item’s commercial-distribution status as In Commercial Distribution. The FDA record also indicates this device is single-use, sterile, though packaging and dating should always be verified on the physical unit received. Reach out if you need help confirming compatibility with your existing equipment or want to explore backorder alternatives. You can also look up this GTIN directly in the FDA AccessGUDID database for the full manufacturer record.

If SKU 519650 is currently on backorder elsewhere, Class 1 Inventory may already have it in stock or know of a comparable substitute within the same category. We work with buyers across ALTIS and other manufacturer lines to keep procurement moving, and we buy back unused surplus inventory as well.

Specifications

• Catalog product name: Coloplast Altis Single Incision Sling System
• SKU / model: 519650
• GTIN / UPC / EAN: 05708932467407
• Brand: ALTIS
• FDA brand name: Altis
• Manufacturer: Coloplast A/S
• FDA commercial distribution status: In Commercial Distribution
• FDA record indicates single use: Yes
• FDA record indicates sterile: Yes