Primary Device ID | 00810074306461 |
NIH Device Record Key | 2e49f6ec-a62d-40c1-a414-2dc9250e8448 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | 8.0mm Drill Bit Cann Hudson Mod 270mm |
Version Model Number | 2004-0032 |
Catalog Number | 2004-0032 |
Company DUNS | 089645059 |
Company Name | Osteocentric Technologies, Inc. |
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 | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 1-800-969-0639 |
quality@osteocentric.com | |
Phone | 1-800-969-0639 |
quality@osteocentric.com | |
Phone | 1-800-969-0639 |
quality@osteocentric.com | |
Phone | 1-800-969-0639 |
quality@osteocentric.com | |
Phone | 1-800-969-0639 |
quality@osteocentric.com | |
Phone | 1-800-969-0639 |
quality@osteocentric.com | |
Phone | 1-800-969-0639 |
quality@osteocentric.com | |
Phone | 1-800-969-0639 |
quality@osteocentric.com | |
Phone | 1-800-969-0639 |
quality@osteocentric.com | |
Phone | 1-800-969-0639 |
quality@osteocentric.com | |
Phone | 1-800-969-0639 |
quality@osteocentric.com | |
Phone | 1-800-969-0639 |
quality@osteocentric.com | |
Phone | 1-800-969-0639 |
quality@osteocentric.com | |
Phone | 1-800-969-0639 |
quality@osteocentric.com |
Outer Diameter | 8 Millimeter |
Outer Diameter | 8 Millimeter |
Outer Diameter | 8 Millimeter |
Outer Diameter | 8 Millimeter |
Outer Diameter | 8 Millimeter |
Outer Diameter | 8 Millimeter |
Outer Diameter | 8 Millimeter |
Outer Diameter | 8 Millimeter |
Outer Diameter | 8 Millimeter |
Outer Diameter | 8 Millimeter |
Outer Diameter | 8 Millimeter |
Outer Diameter | 8 Millimeter |
Outer Diameter | 8 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00810074306461 [Primary] |
HTW | Bit, Drill |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00810074306461]
Moist Heat or Steam Sterilization
[00810074306461]
Moist Heat or Steam Sterilization
[00810074306461]
Moist Heat or Steam Sterilization
[00810074306461]
Moist Heat or Steam Sterilization
[00810074306461]
Moist Heat or Steam Sterilization
[00810074306461]
Moist Heat or Steam Sterilization
[00810074306461]
Moist Heat or Steam Sterilization
[00810074306461]
Moist Heat or Steam Sterilization
[00810074306461]
Moist Heat or Steam Sterilization
[00810074306461]
Moist Heat or Steam Sterilization
[00810074306461]
Moist Heat or Steam Sterilization
[00810074306461]
Moist Heat or Steam Sterilization
[00810074306461]
Moist Heat or Steam Sterilization
[00810074306461]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-05-23 |
Device Publish Date | 2025-05-15 |
00810074308984 - 11 X 75mm LAG FASTENER | 2025-09-30 11 X 75mm LAG FASTENER |
00810074309974 - 11 X 80mm LAG FASTENER | 2025-09-30 11 X 80mm LAG FASTENER |
00810074309981 - 11 X 85mm LAG FASTENER | 2025-09-30 11 X 85mm LAG FASTENER |
00810074309998 - 11 X 90mm LAG FASTENER | 2025-09-30 11 X 90mm LAG FASTENER |
00810189110007 - 11 X 95mm LAG FASTENER | 2025-09-30 11 X 95mm LAG FASTENER |
00810189110014 - 11 X 100mm LAG FASTENER | 2025-09-30 11 X 100mm LAG FASTENER |
00810189110021 - 11 X 105mm LAG FASTENER | 2025-09-30 11 X 105mm LAG FASTENER |
00810189110038 - 11 X 110mm LAG FASTENER | 2025-09-30 11 X 110mm LAG FASTENER |