Primary Device ID | 00810633020326 |
NIH Device Record Key | b77687f3-d5f2-48e6-be4d-e56c9336d8e0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | HammerLock |
Version Model Number | S-240QD |
Company DUNS | 792619009 |
Company Name | Biomedical Enterprises, 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 | true |
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 |
Phone | 210-881-0064 |
aknight@bme-tx.com | |
Phone | 210-881-0064 |
aknight@bme-tx.com | |
Phone | 210-881-0064 |
aknight@bme-tx.com | |
Phone | 210-881-0064 |
aknight@bme-tx.com | |
Phone | 210-881-0064 |
aknight@bme-tx.com | |
Phone | 210-881-0064 |
aknight@bme-tx.com | |
Phone | 210-881-0064 |
aknight@bme-tx.com | |
Phone | 210-881-0064 |
aknight@bme-tx.com | |
Phone | 210-881-0064 |
aknight@bme-tx.com | |
Phone | 210-881-0064 |
aknight@bme-tx.com | |
Phone | 210-881-0064 |
aknight@bme-tx.com | |
Phone | 210-881-0064 |
aknight@bme-tx.com | |
Phone | 210-881-0064 |
aknight@bme-tx.com | |
Phone | 210-881-0064 |
aknight@bme-tx.com | |
Phone | 210-881-0064 |
aknight@bme-tx.com | |
Phone | 210-881-0064 |
aknight@bme-tx.com |
Outer Diameter | 2.4 Millimeter |
Outer Diameter | 2.4 Millimeter |
Outer Diameter | 2.4 Millimeter |
Outer Diameter | 2.4 Millimeter |
Outer Diameter | 2.4 Millimeter |
Outer Diameter | 2.4 Millimeter |
Outer Diameter | 2.4 Millimeter |
Outer Diameter | 2.4 Millimeter |
Outer Diameter | 2.4 Millimeter |
Outer Diameter | 2.4 Millimeter |
Outer Diameter | 2.4 Millimeter |
Outer Diameter | 2.4 Millimeter |
Outer Diameter | 2.4 Millimeter |
Outer Diameter | 2.4 Millimeter |
Outer Diameter | 2.4 Millimeter |
Outer Diameter | 2.4 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00810633020326 [Primary] |
HTW | Bit, Drill |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2020-05-07 |
Device Publish Date | 2015-10-24 |
00810633021392 | Hammerlock Angled X-Type Large |
00810633021385 | Hammerlock X-Type Large |
00810633021378 | Hammerlock implant for DIP |
00810633021361 | Medium, 19mm length Nitinol Intramedullary Implant |
00810633020371 | Hammerlock with mosquito forceps |
00810633020326 | Sterile 2.4mm Drill Bit |
00810633020319 | Sterile 2.0mm Drill Bit |
00810633020074 | Hammerlock Angled X-Type Small 16mm |
00810633020067 | Hammerlock X-Type Small |
00810633020050 | Hammerlock X-Type Petite |
00810633020043 | Hammerlock Angled X-Type Medium 19 |
00810633020036 | Hammerlock Angled X-Type Large |
00810633020029 | Hammerlock X-Type Large |
00810633020012 | Hammerlock implant for DIP |
00810633020005 | Medium, 19mm length Nitinol Intramedullary Implant |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
HAMMERLOCK 88874696 not registered Live/Pending |
Depuy Synthes, Inc. 2020-04-16 |
HAMMERLOCK 87082891 not registered Dead/Abandoned |
Church & Dwight Co., Inc. 2016-06-24 |
HAMMERLOCK 76703118 3902409 Live/Registered |
DEPUY SYNTHES, INC. 2010-05-26 |
HAMMERLOCK 74502086 not registered Dead/Abandoned |
Jaleco USA, Inc. 1994-03-16 |
HAMMERLOCK 74452893 1858517 Dead/Cancelled |
HAMMERLOCK INDUSTRIES, INC. 1993-11-01 |
HAMMERLOCK 74331787 1967157 Live/Registered |
JACOBS CHUCK MANUFACTURING COMPANY, THE 1992-11-16 |
HAMMERLOCK 73592458 1443896 Dead/Cancelled |
HAMMERLOCK CORP. 1986-04-09 |