Archon
- Primary DI
- 00887517203823
- Brand
- Archon
- Company
- Nuvasive, Inc.
- Model
- 8780216
- Device description
- Archon Screw, 4.0x16mm Self-Drill Var
- Published
- 2016-05-27
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- Single use
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| KWQ | APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| KWQ | Appliance, Fixation, Spinal Intervertebral Body | Orthopedic | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K131025 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00887517203823 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00887517203823 | 00887517203823 | 887517203823 | 0887517203823 |
GMDN Terms#
| Term | Definition |
|---|---|
| Cardiopulmonary resuscitation mask, single-use | A flexible, form-shaped device that is placed over a patient's mouth to administer "mouth-to-mask" exhaled air from the user to the patient during cardiopulmonary resuscitation (CPR). The device is designed to replace "mouth-to-mouth" resuscitation therefore reducing the risk of cross-contamination; it is also used on manikins by students during CPR training. The device typically consists of the mask with a mouthpiece and a non-rebreathing valve and/or bacteria filter. Also referred to as a pocket face mask, it is typically used by emergency medical services (EMS) or as part of first aid kits. This is a single-use device. |
Sterilization Methods#
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts#
| Phone | |
|---|---|
| +1(858)909-1800 | RA_UDI@nuvasive.com |
| +1800-475-9131 | nuvainfo@globusmedical.com |
Regulatory Flags#
- DUNS number
- 053950783
- Device count
- 1
- Lot or batch
- true
- Sterilization required before use
- true
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 00887517614360 | Propel | 5020001 | 2015-09-24 | |
| 00887517614377 | Propel | 5020005 | 2015-09-24 | |
| 00887517614384 | Propel | 5020010 | 2015-09-24 | |
| 00887517939951 | AttraX | 5015110 | 2018-06-05 | |
| 00887517939968 | AttraX | 5015120 | 2018-06-05 | |
| 00887517939975 | AttraX | 5015130 | 2018-06-05 | |
| 00887517939982 | AttraX | 5015103 | 2018-06-05 | |
| 00887517939999 | AttraX | 5015104 | 2018-06-05 | |
| 00887517940001 | AttraX | 5015106 | 2018-06-05 | |
| 00887517940018 | AttraX | 5015101 | 2018-06-05 | |
| 00887517940025 | AttraX | 5015102 | 2018-06-05 | |
| 00887517970435 | Propel | 5020205 | 2018-12-20 | |
| 00887517970442 | Propel | 5020205994 | 2018-12-20 | |
| 00887517970459 | Propel | 5020210 | 2018-12-20 | |
| 00887517970466 | Propel | 5020210994 | 2018-12-20 | |
| 00887517970473 | Propel | 5020301 | 2018-12-20 | |
| 00887517970480 | Propel | 5020301994 | 2018-12-20 | |
| 00887517970497 | Propel | 5020305 | 2018-12-20 | |
| 00887517971500 | Propel | 5020305994 | 2018-12-20 | |
| 00887517971517 | Propel | 5020310 | 2018-12-20 |
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