Barre Prostate Retractor
The Barre Prostate Retractor follows the BARRE pattern and is a prostate retractor from the Aesculap surgical instrument range, catalogued under Retractors → Prostate Retractors. It has an overall length of 14 1/4″ (360.00 mm). It is intended for urological procedures, supporting exposure of the urethral and prostatic field. Every specification shown is taken directly from the Aesculap catalogue (source page 750); no attributes have been inferred, and it is tracked internally under registry ID REG-080153. Pricing is provided on request through the inquiry system; submit a Request a Quote for current availability, lead time, and commercial terms.
2-year warranty
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The Barre Prostate Retractor is a prostate retractor within the Aesculap Retractors range, classified under Surgical Instruments → Retractors → Prostate Retractors. It carries the BARRE pattern designation, a named instrument pattern used in the catalogue to identify a specific, repeatable design geometry so that clinical and procurement teams can reliably reorder the same configuration. As a retractor, its role is to hold back tissue and maintain exposure of the operative field, and this instrument is oriented toward urological procedures, where it supports exposure of the urethral and prostatic field.
In terms of design characteristics, the instrument has an overall catalogued length of 14 1/4″ (360.00 mm), recorded in both imperial and metric units. Only the attributes explicitly printed in the source catalogue are reproduced here; no dimensions, materials, or finishes have been inferred beyond the printed record.
This is a standalone product represented by the single catalogue reference BT680R. It is ordered as one configuration; the specification above reflects the complete printed catalogue record for this item.
The key technical specifications, as recorded in the catalogue, are: Pattern / Design: BARRE; Instrument Type: Prostate Retractor; Category: Retractors; Subcategory: Prostate Retractors; Length: 14 1/4″ (360.00 mm); Registry ID: REG-080153; Manufacturer Reference: Aesculap AG / B. Braun.
In terms of application, the instrument type indicates use in urological procedures. As a prostate retractor it is applied to exposure of the urethral and prostatic field, providing and maintaining exposure while the surgeon works. These application areas follow directly from the instrument’s catalogued type designation; the catalogue does not enumerate specific procedures, and the definitive procedural suitability, sterilisation parameters, and compatibility should be confirmed against the manufacturer’s documentation for the relevant reference.
For ordering, quote catalogue reference BT680R. The website operates as a B2B inquiry platform and does not publish prices online; submit a Request a Quote or use Send Inquiry / Contact Us to obtain availability, lead time, and commercial terms.
For identification and traceability, this record is linked to its origin in the printed Aesculap catalogue at page 750, and every specification reproduced here is taken verbatim from that source. The instrument is named in the catalogue with both an English designation and a German designation, reflecting the bilingual nature of the source; the BARRE pattern designation provides an additional, standardised way to reference the specific geometry. Internally the product is tracked under registry ID REG-080153, which keeps the catalogue reference, the product record, and any downstream store listing consistently associated. This traceability matters in a procurement context because it lets a buyer confirm that a quoted or received item corresponds exactly to the catalogued specification.
Regarding material, reprocessing, and regulatory status, the source catalogue entry for this item does not print a material specification. Aesculap reusable retractors of this class are generally manufactured in surgical-grade stainless steel, but the definitive material, surface finish, sterilisation method, and reprocessing parameters for a specific reference should be verified against the manufacturer’s instructions for use rather than assumed. No regulatory clearance, certification, or performance claim is made here; any such status should be confirmed with the manufacturer or authorised distributor for the destination market. This conservative approach keeps the listing accurate and avoids overstating what the catalogue records.
When selecting this instrument, buyers should confirm that its catalogued type and dimensions match the intended surgical access and anatomy. As a single-reference product it is ordered directly by its catalogue number, which keeps quoting, delivery, and inventory management unambiguous.
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