NA
- Primary DI
- H6795304130
- Brand
- NA
- Company
- SYNTHES (U.S.A.) LP
- Model
- 530.413
- Catalog number
- 530413
- Device description
- CABLE FOR COMPARTMENTAL PRESSURE MONITORING SYSTEM
- Published
- 2016-12-31
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- false
- Single use
- false
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| LXC | MONITOR, PRESSURE, INTRACOMPARTMENTAL |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| LXC | Monitor, Pressure, Intracompartmental | Unknown | U |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K031555 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 10886982239914 | Primary | GS1 | 0 | |
| H6795304130 | Secondary | HIBCC | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized |
|---|---|
| 10886982239914 | 10886982239914 |
GMDN Terms#
| Term | Definition |
|---|---|
| Compartmental-pressure monitoring system, reusable | An assembly of devices designed to measure and display, periodically or continuously, the interstitial pressure in a closed fascial compartment of muscle. It typically consists of a battery-powered, hand-held, pressure-measuring instrument with a display and connected devices used to access the muscle compartment (e.g., transducing probe, extension cable). It is intended to assess chronic and/or acute compartmental syndrome, a condition of increased intra-compartmental pressures from swelling within muscle compartments and tendon sheaths due to trauma. This is a reusable device. |
Sterilization Methods#
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts#
| Phone | |
|---|---|
| +1(800)255-2500 | xx@xx.xx |
Regulatory Flags#
- DUNS number
- 832637081
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- false
- HCT/P
- false
- Kit
- false
- Combination product
- false
- Lot or batch
- true
- Serial number
- false
- Manufacturing date on label
- false
- Expiration date on label
- false
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- true
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 10705034711874 | ATB | 03.601.110 | 03601110 | 2016-12-31 |
| 10705034711881 | ATB | 03.601.111 | 03601111 | 2016-12-31 |
| 10705034711898 | ATB | 03.601.112 | 03601112 | 2016-12-31 |
| 10705034711904 | ATB | 03.601.113 | 03601113 | 2016-12-31 |
| 10705034711911 | ATB | 03.601.114 | 03601114 | 2016-12-31 |
| 10705034711928 | ATB | 03.601.115 | 03601115 | 2016-12-31 |
| 10705034711935 | ATB | 03.601.116 | 03601116 | 2016-12-31 |
| 10705034711942 | ATB | 03.601.117 | 03601117 | 2016-12-31 |
| 10705034711959 | ATB | 03.601.118 | 03601118 | 2016-12-31 |
| 10705034711966 | ATB | 03.601.140 | 03601140 | 2016-12-31 |
| 10705034711973 | ATB | 03.601.142 | 03601142 | 2016-12-31 |
| 10705034711980 | ATB | 03.601.144 | 03601144 | 2016-12-31 |
| 10705034711997 | ATB | 03.601.146 | 03601146 | 2016-12-31 |
| 10705034712000 | ATB | 03.601.148 | 03601148 | 2016-12-31 |
| 10705034712017 | ATB | 03.601.150 | 03601150 | 2016-12-31 |
| 10705034712024 | ATB | 03.601.152 | 03601152 | 2016-12-31 |
| 10705034712031 | ATB | 03.601.154 | 03601154 | 2016-12-31 |
| 10705034712048 | ATB | 03.601.156 | 03601156 | 2016-12-31 |
| 10705034712055 | ATB | 03.601.170 | 03601170 | 2016-12-31 |
| 10705034712062 | ATB | 03.601.172 | 03601172 | 2016-12-31 |
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