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Listing: #5195003
V. Mueller Precision Ophthalmic Eye Micro Surgery Surgical Instruments Set VU2935, OP3495, 5-1603, MDS1821605, 11-2-6782, 0S1079-007
This V. Mueller Precision Ophthalmic Eye Micro Surgery Surgical Instruments Set is in great working and cosmetic condition.
What's Included:
V. Mueller Towel Clamps, Non-Perforated 4; (REF - VU2935); Qty: 1
V. Mueller Needle Holder Vital Halsey 5 Straight; (REF OP7511); Qty: 1
V. Mueller Towel Clamp, 3.5; (REF VU2900); Qty: 1
V. Mueller Septum Elevator Freer 7-3/4; (REF RH750); Qty: 1
V. Mueller Key Periosteal Elevator, 8-1/4; (REF 0S1079-007); Qty: 1
V. Mueller McPherson Micro Iris, and Suture Forcep. Smooth Tip, Straight Jaws, 3 1/4" (83mm); (REF OP3495); Qty: 1
Precision Lieberman Adult Round-Wire Speculum With Adjustable Mechanism; (REF 11-2-6782); Qty: 1
Precision Graefe Strabismis Hook; (REF 5-1603); Qty: 1
Precision Jameson Muscle Hook; (REF 5-1697); Qty: 1
Precision Knapp Lacrimal Retractor 4 Prongs Blunt Overall Length 5" (127mm); (REF 5-1649); Qty: 1
Knig Bishop-Harmon Extra-Delicate Tissue Forceps with 1x2 Teeth and 0.3 mm Tips, 3-3/8" (8.6 cm); (REF - MDS4294208 ); Qty: 1
Knig Nasal Tenacula Joseph Delicate Skin Hook 2-Prong 5mm 6.25L (REF - MDS1821605); Qty: 2
Storz Vannas Capsulotomy Scissors Angled 6mm; (REF - 3388); Qty: 1
Storz Berke-Jaeger Lid Plate; (REF - E1069); Qty: 1
Unbranded Instruments Qty: 19
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This device has been carefully reviewed and conforms withs Prescription devices policy.
To the best of our knowledge and abilities, this device has been cleaned and handled in accordance with manufacturers instructions.
"The sale of this item may be subject to regulation by the U.S. Food and Drug Administration and state and local regulatory agencies. If so, do not buy this item unless you are an authorized purchaser. If the item is subject to FDA regulation, I will verify your status as an authorized purchaser of this item before shipping of the item."
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Also pers Prescription Devices Policy, we must provide the following information about our company for listings of devices that may fall under this FDA guideline:
, d.b.a,
Casselberry, Florida
[phone removed by] Office Number