NA
- Primary DI
- 10705034798455
- Brand
- NA
- Company
- SYNTHES (U.S.A.) LP
- Model
- 690.038
- Catalog number
- 690038
- Device description
- CAVITY CREATION CURETTE SET GRAPHIC CASE
- Published
- 2016-12-31
- Public version status
- Update
- Distribution status
- Not 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 |
|---|---|
| FSM | TRAY, SURGICAL, INSTRUMENT |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| FSM | Tray, Surgical, Instrument | General, Plastic Surgery | 1 |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 10705034798455 | Primary | GS1 | 0 | |
| H9816900380 | Secondary | HIBCC | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized |
|---|---|
| 10705034798455 | 10705034798455 |
GMDN Terms#
| Term | Definition |
|---|---|
| Instrument tray, reusable | A container intended to provide a suitable platform for placing/containing many medical/surgical/dental instruments and related items for use during a clinical procedure; it might, in addition, be used during, but not dedicated to, reprocessing/sterilization procedures. It is a receptacle in one of a variety of designs, typically with moulded positions for placing the instruments; it might include a lid and/or removable identification tags. 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
- true
- 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 |
|---|---|---|---|---|
| 10886982249210 | NA | 60.550.040 | 60550040 | 2017-02-20 |
| 10886982239884 | NA | 530.412 | 530412 | 2016-12-31 |
| 10886982192172 | NA | 329.722 | 329722 | 2017-02-20 |
| 10886982192295 | LC-DCP | 329.918 | 329918 | 2017-02-20 |
| 10886982201461 | NA | 398.56 | 39856 | 2017-02-20 |
| 10886982201478 | NA | 398.58 | 39858 | 2017-02-20 |
| 10705034718040 | NA | 03.620.219 | 03620219 | 2018-10-29 |
| 10705034767802 | VentroFix | 304.832 | 304832 | 2016-12-31 |
| 10705034775418 | NA | 389.296 | 389296 | 2016-12-31 |
| 10705034775425 | NA | 389.297 | 389297 | 2016-12-31 |
| 10705034775432 | NA | 389.298 | 389298 | 2016-12-31 |
| 10705034775449 | NA | 389.299 | 389299 | 2016-12-31 |
| 10887587039893 | NA | 338.761 | 338761 | 2016-12-31 |
| 10886982338778 | MAXFRAME | 1100022-01 | 110002201 | 2024-02-05 |
| 10886982338570 | MAXFRAME | 1100011-01 | 110001101 | 2022-04-26 |
| 10886982338587 | MAXFRAME | 1100010-01 | 110001001 | 2022-04-26 |
| 10886982338594 | MAXFRAME | 1100012-01 | 110001201 | 2022-04-26 |
| 10886982338600 | MAXFRAME | 1100007-01 | 110000701 | 2022-04-26 |
| 10886982237217 | NA | 510.161 | 510161 | 2019-02-21 |
| 10887587039305 | NA | 329.37 | 32937 | 2016-12-31 |
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| 08800037575173 | ANAX™ 5.5 SPINAL SYSTEM | CG MedTech Co.,Ltd. | FSM | 2026-09-04 |
| 08800037575180 | ANAX™ 5.5 SPINAL SYSTEM | CG MedTech Co.,Ltd. | FSM | 2026-09-04 |
| 08800037585110 | ANAX™ 5.5 SPINAL SYSTEM | CG MedTech Co.,Ltd. | FSM | 2026-09-04 |
| 07640221370884 | TRYPTIK® Ti | SpineArt SA | FSM | 2026-08-27 |
| 07613327630602 | Mako | MAKO SURGICAL CORP. | FSM | 2026-08-25 |
| 00724995296216 | V. Mueller | Steris Corporation | FSM | 2026-08-21 |
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