Home GUDID 00192896019751 MIKULICZ RETRACTOR
Primary DI 00192896019751
Brand MIKULICZ RETRACTOR
Company SONTEC INSTRUMENTS, INC.
Model 20-0930
Catalog number 20-0930
Device description MIKULICZ RETRACTOR
Published 2018-09-11
Public version status Update
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true Product Codes# Code, Name table Code Name FGN RETRACTOR, NON-SELF-RETAINING
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class FGN Retractor, Non-Self-Retaining Gastroenterology, Urology 1
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 00192896019751 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, UPC-A table Source identifier GTIN-14 normalized UPC-A EAN-13 00192896019751 00192896019751 192896019751 0192896019751
GMDN Terms# Term, Definition table Term Definition Hand-held surgical retractor, reusable A hand-held, non-self-retaining surgical instrument intended to be used to separate/draw aside the margins of a wound/incision to allow access to tissues/organs during open surgery; it is not dedicated to ophthalmic surgery or small nerve/vessel retraction, but may otherwise be clinically dedicated. It includes a shaped/hooked blade with a handle/holding portion and is available in a wide variety of designs, such as a double- or single-ended blade that may be fenestrated (pronged); deep wound retractors are typically designed with a long, curved blade that may also be intended to retract organs; it may include a light. This is a reusable device.
Device Sizes# Type, Value, Unit table Type Value Unit Device Size Text, specify 0 Length 10 Inch
Sterilization Methods# Method table Method "[""Moist Heat or Steam Sterilization"", ""Dry Heat Sterilization""]" Moist Heat or Steam Sterilization;Dry Heat Sterilization
Regulatory Flags# DUNS number 040729840 Device count 1 Premarket exempt true Lot or batch true Sterilization required before use true Other Devices From This Company# Other Devices Sharing Product Codes# Primary DI, Brand, Company table Primary DI Brand Company Product code Published B803NL97020450 ORTHOMED ORTHO-MED, INC. FGN 2026-06-25 B803COD5045680 ORTHOMED ORTHO-MED, INC. FGN 2026-06-23 B803COD5045690 ORTHOMED ORTHO-MED, INC. FGN 2026-06-23 B803COD5045700 ORTHOMED ORTHO-MED, INC. FGN 2026-06-23 B803COD5045710 ORTHOMED ORTHO-MED, INC. FGN 2026-06-23 B803MA1107210 ORTHOMED ORTHO-MED, INC. FGN 2026-06-23 B803MA1107230 ORTHOMED ORTHO-MED, INC. FGN 2026-06-23 B803MA1107370 ORTHOMED ORTHO-MED, INC. FGN 2026-06-23 B803MA1107390 ORTHOMED ORTHO-MED, INC. FGN 2026-06-23 B803MA1108340 ORTHOMED ORTHO-MED, INC. FGN 2026-06-23 B803MA1108360 ORTHOMED ORTHO-MED, INC. FGN 2026-06-23 B803MA1108370 ORTHOMED ORTHO-MED, INC. FGN 2026-06-23 B803NL97020100 ORTHOMED ORTHO-MED, INC. FGN 2026-06-23 B803NL97020110 ORTHOMED ORTHO-MED, INC. FGN 2026-06-23 B803NL97020120 ORTHOMED ORTHO-MED, INC. FGN 2026-06-23 B803NL97020130 ORTHOMED ORTHO-MED, INC. FGN 2026-06-23 B803NL97020140 ORTHOMED ORTHO-MED, INC. FGN 2026-06-23 B803NL97020150 ORTHOMED ORTHO-MED, INC. FGN 2026-06-23 B803NL97020200 ORTHOMED ORTHO-MED, INC. FGN 2026-06-23 B803NL97020210 ORTHOMED ORTHO-MED, INC. FGN 2026-06-23 B803NL97020220 ORTHOMED ORTHO-MED, INC. FGN 2026-06-23 B803NL97020230 ORTHOMED ORTHO-MED, INC. FGN 2026-06-23 B803NL97020240 ORTHOMED ORTHO-MED, INC. FGN 2026-06-23 B803NL97020250 ORTHOMED ORTHO-MED, INC. FGN 2026-06-23 B803NL97020260 ORTHOMED ORTHO-MED, INC. FGN 2026-06-23 B803NL97020300 ORTHOMED ORTHO-MED, INC. FGN 2026-06-23 B803NL97020310 ORTHOMED ORTHO-MED, INC. FGN 2026-06-23 B803NL97020320 ORTHOMED ORTHO-MED, INC. FGN 2026-06-23 B803NL97020330 ORTHOMED ORTHO-MED, INC. FGN 2026-06-23 B803NL97020340 ORTHOMED ORTHO-MED, INC. FGN 2026-06-23
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