Primary Device ID | 00845384017813 |
NIH Device Record Key | fcb2cc23-2ae0-4b3b-856b-9c3369051555 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Anspach Helix |
Version Model Number | S-25SB-HX-G1 |
Catalog Number | S-25SB-HX-G1 |
Company DUNS | 079116867 |
Company Name | Anspach Effort, The |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00845384017813 [Primary] |
ERL | DRILL, SURGICAL, ENT (ELECTRIC OR PNEUMATIC) INCLUDING HANDPIECE |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-12-19 |
Device Publish Date | 2019-12-11 |
00845384017813 | ANSPACH HELIX™ 2.5 mm Fluted Ball, Standard Length |
00845384017806 | ANSPACH HELIX™ 2 mm Fluted Ball, Extended Length |
00845384017790 | ANSPACH HELIX™ 2 mm Fluted Ball, Standard Length |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ANSPACH HELIX 88144797 not registered Live/Pending |
DePuy Synthes, Inc. 2018-10-05 |
ANSPACH HELIX 86566073 not registered Dead/Abandoned |
DePuy Synthes, Inc. 2015-03-17 |