Primary Device ID | 00812301020270 |
NIH Device Record Key | 08aadaa9-487d-4f51-9b75-2e914208bf40 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Biomet SpinalPak / OrthoPak |
Version Model Number | 1067722 |
Catalog Number | 1067722 |
Company DUNS | 050410323 |
Company Name | EBI, LLC |
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 | true |
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 | 1.973.299.9300 |
BTBS.CSORDERS@BIOMET.COM | |
Phone | 1.973.299.9300 |
BTBS.CSORDERS@BIOMET.COM | |
Phone | 1.973.299.9300 |
BTBS.CSORDERS@BIOMET.COM | |
Phone | 1.973.299.9300 |
BTBS.CSORDERS@BIOMET.COM | |
Phone | 1.973.299.9300 |
BTBS.CSORDERS@BIOMET.COM | |
Phone | 1.973.299.9300 |
BTBS.CSORDERS@BIOMET.COM | |
Phone | 1.973.299.9300 |
BTBS.CSORDERS@BIOMET.COM | |
Phone | 1.973.299.9300 |
BTBS.CSORDERS@BIOMET.COM | |
Phone | 1.973.299.9300 |
BTBS.CSORDERS@BIOMET.COM | |
Phone | 1.973.299.9300 |
BTBS.CSORDERS@BIOMET.COM | |
Phone | 1.973.299.9300 |
BTBS.CSORDERS@BIOMET.COM | |
Phone | 1.973.299.9300 |
BTBS.CSORDERS@BIOMET.COM | |
Phone | 1.973.299.9300 |
BTBS.CSORDERS@BIOMET.COM | |
Phone | 1.973.299.9300 |
BTBS.CSORDERS@BIOMET.COM | |
Phone | 1.973.299.9300 |
BTBS.CSORDERS@BIOMET.COM | |
Phone | 1.973.299.9300 |
BTBS.CSORDERS@BIOMET.COM | |
Phone | 1.973.299.9300 |
BTBS.CSORDERS@BIOMET.COM | |
Phone | 1.973.299.9300 |
BTBS.CSORDERS@BIOMET.COM | |
Phone | 1.973.299.9300 |
BTBS.CSORDERS@BIOMET.COM | |
Phone | 1.973.299.9300 |
BTBS.CSORDERS@BIOMET.COM | |
Phone | 1.973.299.9300 |
BTBS.CSORDERS@BIOMET.COM | |
Phone | 1.973.299.9300 |
BTBS.CSORDERS@BIOMET.COM | |
Phone | 1.973.299.9300 |
BTBS.CSORDERS@BIOMET.COM | |
Phone | 1.973.299.9300 |
BTBS.CSORDERS@BIOMET.COM | |
Phone | 1.973.299.9300 |
BTBS.CSORDERS@BIOMET.COM | |
Phone | 1.973.299.9300 |
BTBS.CSORDERS@BIOMET.COM | |
Phone | 1.973.299.9300 |
BTBS.CSORDERS@BIOMET.COM |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00812301020270 [Primary] |
LOF | Stimulator, Bone Growth, Non-Invasive |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2014-09-19 |
00812301020393 | AC ADAPTOR, ALTERNATE |
00812301020386 | AC ADAPTER KIT |
00812301020379 | WALL PLUG ADAPTER KIT |
00812301020362 | AC ADAPTOR, REPLACEMENT |
00812301020331 | 72" LEAD WIRES, REPLACEMENT |
00812301020324 | 48" LEAD WIRES, REPLACEMENT |
00812301020317 | 30" LEAD WIRES, REPLACEMENT |
00812301020300 | 20" LEAD WIRES, REPLACEMENT |
00812301020294 | 12" LEAD WIRES, REPLACEMENT |
00812301020287 | EXTREMITY BAND, REPLACEMENT |
00812301020270 | STIMULATOR HOLSTER, REPLACEMENT |
00812301020263 | BATTERY PACK CHARGER, REPLACEMENT |
00812301020256 | BATTERY PACK, REPLACEMENT |
00812301020201 | ELECTRODES 72R, SOFT TOUCH REPLACEMENT |
00812301020195 | ELECTRODE COVER PATCHES |
00812301020188 | ELECTRODES, LT-4500 |
00880304820852 | ELECTRODES, 63B, SPINALPAK/ORTHOPAK |
00880304820845 | BELT EXTENSION, LARGE, SPINALPAK |