Primary Device ID | 10886982344410 |
NIH Device Record Key | cdc688e0-ea3b-42c5-96b0-7b1c41e512a7 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | SD03.300.100 |
Catalog Number | SD03300100 |
Company DUNS | 486711679 |
Company Name | Synthes GmbH |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | 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)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10886982344410 [Primary] |
HWT | TEMPLATE |
Steralize Prior To Use | true |
Device Is Sterile | false |
[10886982344410]
Moist Heat or Steam Sterilization
[10886982344410]
Moist Heat or Steam Sterilization
[10886982344410]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-02-26 |
Device Publish Date | 2025-02-18 |
10886982344410 - NA | 2025-02-26MAXFRAME CONTROL BOX TEMPLATE |
10886982344410 - NA | 2025-02-26 MAXFRAME CONTROL BOX TEMPLATE |
10886982348333 - NA | 2025-02-26 1.1MM PARALLEL WIRE GUIDE |
10886982348364 - NA | 2025-02-26 1.4MM PARALLEL WIRE GUIDE |
10886982348395 - NA | 2025-02-26 1.6MM PARALLEL WIRE GUIDE |
10886982349088 - NA | 2025-02-26 TERMITE REDUCTION FORCEPS SERRATED JAW |
H6792050550 - NA | 2025-02-20 3.5MM CANNULATED SCREW PARTIALLY THREADED/55MM |
H6794089050 - NA | 2025-02-20 7.3MM TI CANNULATED SCREW 16MM THREAD/105MM |
07612334285515 - VOLT | 2024-12-19 VOLT(TM) PROX HUM IMP & INSTR 1 HIGH 3/3 WIDTH ALUM TRAY |