SURFIX®
GUDID M248SET000ND1
This tray is used for transport and sterilization of the instruments that are not specific to the osteotomy surgery (drilling guides, length gauge, drills, plate benders, hexagonal screwdriver).
NEWDEAL
Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable| Primary Device ID | M248SET000ND1 |
| NIH Device Record Key | e7b88ff5-9679-4862-b8c6-2921f6f6961c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SURFIX® |
| Version Model Number | SET000ND |
| Company DUNS | 536935331 |
| Company Name | NEWDEAL |
| 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 | true |
| Device Combination Product | false |
| Single Use | false |
| 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 | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
Customer Support Contacts
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10381780042822 [Primary] |
| HIBCC | M248SET000ND1 [Secondary] |
FDA Product Code
| FSM | TRAY, SURGICAL, INSTRUMENT |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[M248SET000ND1]
Moist Heat or Steam Sterilization
[M248SET000ND1]
Moist Heat or Steam Sterilization
[M248SET000ND1]
Moist Heat or Steam Sterilization
[M248SET000ND1]
Moist Heat or Steam Sterilization
[M248SET000ND1]
Moist Heat or Steam Sterilization
[M248SET000ND1]
Moist Heat or Steam Sterilization
[M248SET000ND1]
Moist Heat or Steam Sterilization
[M248SET000ND1]
Moist Heat or Steam Sterilization
[M248SET000ND1]
Moist Heat or Steam Sterilization
[M248SET000ND1]
Moist Heat or Steam Sterilization
[M248SET000ND1]
Moist Heat or Steam Sterilization
[M248SET000ND1]
Moist Heat or Steam Sterilization
[M248SET000ND1]
Moist Heat or Steam Sterilization
[M248SET000ND1]
Moist Heat or Steam Sterilization
[M248SET000ND1]
Moist Heat or Steam Sterilization
[M248SET000ND1]
Moist Heat or Steam Sterilization
[M248SET000ND1]
Moist Heat or Steam Sterilization
[M248SET000ND1]
Moist Heat or Steam Sterilization
[M248SET000ND1]
Moist Heat or Steam Sterilization
[M248SET000ND1]
Moist Heat or Steam Sterilization
[M248SET000ND1]
Moist Heat or Steam Sterilization
[M248SET000ND1]
Moist Heat or Steam Sterilization
[M248SET000ND1]
Moist Heat or Steam Sterilization
[M248SET000ND1]
Moist Heat or Steam Sterilization
[M248SET000ND1]
Moist Heat or Steam Sterilization
[M248SET000ND1]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2021-07-08 |
| Device Publish Date | 2017-05-26 |
On-Brand Devices [SURFIX®]
| M248MA007ND1 | The drilling guide is placed in the plate on the bone and is used to guide the drilling of the b |
| M248MA006ND1 | The drilling guide is placed in the plate on the bone and is used to guide the drilling of the b |
| M248219665ND1 | The drilling guide is used to guide the drills while preparing the holes for the 6.5 mm fixation |
| M248219645ND1 | The drilling guide is used to guide the drills while preparing the holes for the 4.5 mm fixation |
| M248219635ND1 | The drilling guide is used to guide the drills while preparing the holes for the 3.5 mm fixation |
| M248219035ND1 | The SURFIX® ALPHA drilling guide for variable angle screws is used to guide the drills while pr |
| M248219027ND1 | The SURFIX® ALPHA drilling guide is used to guide the drills while preparing the holes for the |
| M248SET101ND1 | This lid is used to ensure closing of both trays numbers SET000ND and SET100ND. |
| M248SET100ND1 | This tray is used for transport and sterilization of the instruments that are specific to the os |
| M248SET000ND1 | This tray is used for transport and sterilization of the instruments that are not specific to th |
| M248286340SND1 | Stainless steel Newdeal sterile locking system fixation consists of screws and washers. This sys |
| M248286340ND1 | Stainless steel Newdeal non sterile locking system fixation consists of screws and washers. This |
| M248286338SND1 | Stainless steel Newdeal sterile locking system fixation consists of screws and washers. This sys |
| M248286338ND1 | Stainless steel Newdeal non sterile locking system fixation consists of screws and washers. This |
| M248286336SND1 | Stainless steel Newdeal sterile locking system fixation consists of screws and washers. This sys |
| M248286336ND1 | Stainless steel Newdeal non sterile locking system fixation consists of screws and washers. This |
| M248529061ND1 | This K-Wire of diameter 2.5 mm and of length 250 mm is used to guide the instrumentation and the |
Trademark Results [SURFIX]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 SURFIX 97788707 not registered Live/Pending |
Surfix Incorporated 2023-02-09 |
 SURFIX 87428160 5339969 Live/Registered |
PENETRON INTERNATIONAL LTD. 2017-04-27 |
 SURFIX 79097131 4120156 Live/Registered |
TTS Tooltechnic Systems AG & Co. KG 2010-12-30 |
 SURFIX 79006527 3324725 Live/Registered |
NEWDEAL 2004-06-07 |
 SURFIX 73325308 1223054 Live/Registered |
Helena Chemical Company 1981-08-26 |
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