Uncoated Surgipro™ sutures (clear or pigmented) are inert, nonabsorbable, sterile sutures composed of an isotactic crystalline stereoisomer of polypropylene (a synthetic linear polyolefin) and polyethylene.
The advanced extrusion process of the polypropylene molecule gives the suture:
Surgipro™ polypropylene sutures are indicated for use in general soft tissue approximation and/or ligation, including use in cardiovascular, ophthalmic, and neurological surgery.
Structure | Monofilament |
Suture Type | Non-Absorbable |
Composition | Surgipro™ – Polypropylene Surgipro™ II – Polypropylene with ethylene |
Coating | Uncoated |
Colour | Blue, Clear |
Tensile Strength | Permenet |
Absorption Profile | Permanent |
Sizes | Surgipro™ suture: Sizes 10-0, 6-0, 2-0 through 2 Surgipro™ II suture: Sizes 8-0 to 3-0 |
Indications | Surgipro™ and Surgipro™ II polypropylene suture is indicated for use in general soft tissue approximation and/or ligation, including use in cardiovascular, ophthalmic and neural tissue. |
Contraindications | None known |
Box Questions | 1, 2 or 3 dozen |
Surgipro™ and Surgipro™ II codes can be identified with codes beginning with: SP, CP, 3CP, P ,VP, VPF, X, GP |
1. Based on validation report #RE00171206 with 13 Surgeon Evaluation of Surgipro ™ II CV Suture Strength. 09/18/2018.
2. Based on validation report #RE00073496, Optimized Diameter Surgipro ™ II 4-0 Evaluation. 01/24/2017.
3. Based on validation report #RE00115198, Surgipro ™ II 4-0 Top Performing DOE Sample Validation. 10/10/2017.
4. Based on validation report #RE00115202, Optimized Diameter Surgipro ™ II Sizes 5-0, 6-0, and 7-0 Validation. 09/28/2017.
5. Based on validation report #RE00167893, Surgipro ™ II 5-0 DOE Sample Validation. 09/04/2018.
6. Based on validation report #RE00167895, Surgipro ™ II 7-0 DOE Sample Validation. 09/25/2018.