0116311 – Bard 3D MAX MID Anatomical Mesh LEFT

About the Bard 3D MAX MID Anatomical Mesh LEFT — SKU 0116311

SKU 0116311 corresponds to the Bard 3D MAX MID Anatomical Mesh LEFT from Bard, manufactured by Davol Inc. According to its FDA GUDID device record, this item is described as “3dmax mid anatomical mesh, 10 cm x 16 cm (4″ x 6″), large, left”. We include this FDA-sourced identification alongside the standard catalog details so purchasing and receiving teams can verify the exact device before it ships.

Product Details

The Bard 3DMax MID Anatomical Mesh Left is engineered for robotic and laparoscopic inguinal hernia repair. Its anatomical design helps simplify placement while providing reliable support and reinforcement throughout the procedure.

When comparing this item to similar products from other manufacturers, use SKU 0116311 and GTIN 00801741200755 to confirm you’re matching the exact configuration your facility needs.

0116311 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 0116311 is currently on backorder elsewhere, Class 1 Inventory may already have it in stock or know of a comparable substitute within Surgical Mesh. We work with buyers across Bard and other manufacturer lines to keep procurement moving, and we buy back unused surplus inventory as well.

Specifications

• Catalog product name: Bard 3D MAX MID Anatomical Mesh LEFT
• SKU / model: 0116311
• GTIN / UPC / EAN: 00801741200755
• Brand: Bard
• FDA brand name: 3DMAX
• Manufacturer: Davol Inc.
• FDA commercial distribution status: In Commercial Distribution
• FDA record indicates single use: Yes
• FDA record indicates sterile: Yes