Curaplex
- Primary DI
- 00810094579531
- Brand
- Curaplex
- Company
- BOUND TREE MEDICAL, LLC
- Model
- OneScope Pro
- Catalog number
- 3034025
- Device description
- One Scope Pro -Adult Direct Mac 3 Blade
- Published
- 2025-08-07
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- true
- Single use
- true
Product Codes#
| Code | Name |
|---|---|
| LRC | INSTRUMENT, ENT MANUAL SURGICAL |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| LRC | Instrument, Ent Manual Surgical | Ear, Nose, Throat | 1 |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00810094579531 | Package | GS1 | 25 | In Commercial Distribution |
| 00810094578305 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00810094579531 | 00810094579531 | 810094579531 | 0810094579531 |
| 00810094578305 | 00810094578305 | 810094578305 | 0810094578305 |
GMDN Terms#
| Term | Definition |
|---|---|
| Video intubation laryngoscope blade | A rigid, blade-like component of a bladed video intubation laryngoscope intended to be inserted into the oral cavity to manipulate the tongue, preventing it from obstructing the oropharynx and enabling a clear view of the trachea for the insertion of an endotracheal (ET) tube prior to the delivery of inhalation anaesthesia and/or ventilation. It has an electronic camera at its distal end to transmit anatomical images by a video system to a connected video intubation laryngoscope handle/monitor. This is a single-use device. |
Sterilization Methods#
| Method |
|---|
| Ethylene Oxide |
Regulatory Flags#
- DUNS number
- 070556204
- 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
- true
- Expiration date on label
- true
- 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 |
|---|---|---|---|---|
| 00810094575809 | Curaplex | 680152-KIT | 680152-KIT | 2023-04-30 |
| 00815277028059 | Curaplex | 8600-ATFMLOK | 2016-12-14 | |
| 00815277029377 | Curaplex | 680150-KIT | 680150-KIT | 2018-12-15 |
| 01999720000003 | Curaplex Advanced Hemostatic Gauze | 4in x 4in(10cm x 10cm) | CAHG-4X4 | 2025-11-25 |
| 01999720000027 | Curaplex Advanced Hemostatic Gauze | 3in x 1.6 Yds (7.6cm x 150 cm) | CAHG-R5 | 2025-11-25 |
| 01999720000041 | Curaplex Advanced Hemostatic Gauze | 3in x 3.2Yds (7.6cm x 300 cm) | CAHG-Z10 | 2025-11-25 |
| 01999720000065 | Curaplex® | 8600-01555 | 8600-01555 | 2025-11-13 |
| 01999720000263 | Curaplex | 670070-KIT | 670070-KIT | 2025-11-25 |
| 00810071638619 | CURAPLEX | S1137 | 301-S1137 | 2023-03-30 |
| 00817617023052 | Curaplex | 3141-91010 | 3141-91010 | 2017-09-04 |
| 00817617023069 | Curaplex | 3141-91012 | 3141-91012 | 2017-09-04 |
| 00817617023083 | Curaplex | 3141-91014 | 3141-91014 | 2017-09-04 |
| 00817617023335 | Curaplex | 36111 | 36111 | 2017-09-04 |
| 00199972000085 | Curaplex | 8600-01535 | 8600-01535 | 2026-01-23 |
| 00199972000092 | Curaplex | 8600-01536 | 8600-01536 | 2026-01-23 |
| 00199972000108 | Curaplex | 8600-01537 | 8600-01537 | 2026-01-23 |
| 00199972000115 | Curaplex | 8600-01538 | 8600-01538 | 2026-01-23 |
| 00199972000122 | Curaplex | 8600-01539 | 8600-01539 | 2026-01-23 |
| 00199972000139 | Curaplex | 8600-01540 | 8600-01540 | 2026-01-23 |
| 00199972000146 | Curaplex | 8600-01541 | 8600-01541 | 2026-01-23 |
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