Home GUDID 00844505014762 BONE WAX APPLICATOR
Primary DI 00844505014762
Brand BONE WAX APPLICATOR
Company Grace Medical, Inc.
Model 900-001
Device description BONE WAX APPLICATOR DOUBLE-ENDED
Published 2026-08-27
Public version status New
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true
OTC false
Sterile true
Single use true Product Codes# Code, Name table Code Name LRC Instrument, Ent Manual Surgical
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class LRC Instrument, Ent Manual Surgical Ear, Nose, Throat 1
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 10844505014639 Package GS1 5 In Commercial Distribution 00844505014762 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 10844505014639 10844505014639 00844505014762 00844505014762 844505014762 0844505014762
GMDN Terms# Term, Definition table Term Definition General-purpose surgical spatula A hand-held manual surgical instrument designed to manipulate tissue during various types of surgical interventions. It typically consists of a flat blunt blade (no sharp edges) that is double-ended (a blade at either end) and is not constructed for one particular part of the anatomy or clinical specialty. It is usually made of high-grade stainless steel and is available with a variety of blade designs, e.g., curved and flat or straight and flat with rounded ends; some blade types may be more right-angled. The handle will be formed from its middle section and may be more prominent/serrated. This is a reusable device.
Regulatory Flags# DUNS number 030849173 Device count 1 DM exempt false Premarket exempt true HCT/P false Kit false Combination product false Lot or batch true Serial number false Manufacturing date on label true Expiration date on label true Donation ID number false Contains natural rubber latex false No natural rubber latex false Sterilization required before use false Other Devices From This Company# Primary DI, Brand, Model table Primary DI Brand Model Catalog Published 00844505012508 Cartilage MACROTOME Handle 990-103 2021-10-29 00844505012515 Cartilage MACROTOME Module 990-104 2021-10-29 00844505012522 Cartilage MACROTOME Tissue Support 990-106 2021-10-29 00844505007139 CARTILAGE MICROTOME 990-001 2018-09-21 00844505009010 CARTILAGE MICROTOME MODULE 990-004 2018-09-21 00844505010399 CARTILAGE MICROTOME HANDLE 990-003 2018-09-21 00844505010405 TISSUE SUPPORT DIAL 990-006 2018-09-21 00844505014786 FEATHERVAC, ECLIPSE 906-102 2026-08-18 00844505014793 FEATHERVAC, ECLIPSE FLAT RIBBON 906-103 2026-08-18 00844505014625 HOUGH FLAP KNIFE 999-204 2026-03-27 00844505014632 THOMASSIN DISSECTOR 999-205 2026-03-27 00844505010269 TITANIUM/FLUOROPLASTIC PISTON 409-600 2026-02-03 00844505014526 GRACE PISTON 412-525 2026-01-07 00844505014533 GRACE PISTON 412-550 2026-01-07 00844505014540 GRACE PISTON 412-575 2026-01-07 00844505012249 EndoEar™ ENDOSCOPE, 3MM X 150MM, 0 DEG. EE-0300 2019-12-05 00844505012256 EndoEar™ ENDOSCOPE, 3MM X 150MM, 30 DEG. EE-0330 2019-12-05 00844505012263 EndoEar™ ENDOSCOPE, 3MM X 150MM, 45 DEG. EE-0345 2019-12-05 00844505012270 EndoEar™ ENDOSCOPE, 3MM X 150MM, 70 DEG. EE-0370 2019-12-05 00844505014694 SKULL BASE 999-SB1 2025-09-26
Other Devices Sharing Product Codes#