Curaplex
- Primary DI
- 00815277023047
- Brand
- Curaplex
- Company
- BOUND TREE MEDICAL, LLC
- Model
- 10-83611
- Device description
- Curaplex Select IV Admin Set, 10 Drop, 83 in, 1 LL Site, 1 PP Site, 6 in Ext Set w/Pinch Clamp 50/cs
- Published
- 2016-12-14
- Public version status
- Update
- 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 |
|---|---|
| FPA | Set, administration, intravascular |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| FPA | Set, Administration, Intravascular | General Hospital | 2 |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00815277023047 | Package | GS1 | 50 | In Commercial Distribution |
| 00815277023030 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00815277023047 | 00815277023047 | 815277023047 | 0815277023047 |
| 00815277023030 | 00815277023030 | 815277023030 | 0815277023030 |
GMDN Terms#
| Term | Definition |
|---|---|
| Non-absorbing intravenous administration set | A collection of sterile devices designed for the intravenous (IV) administration of solutions and manufactured with low-absorption plastics to avoid partial absorption of the components of the infused solutions. It typically consists of plastic tubes made of or lined with non absorbing plastics [e.g., polyethylene (PE), Teflon], to avoid solution contact with polyvinyl chloride (PVC) components; it also includes a check valve, a roller clamp, a Y-site connector, and Luer adaptors. The set is mainly used in high-flow infusion pumps for administration of solutions containing products (e.g., nitroglycerin) that are absorbed by PVC materials. This is a single-use device. |
Sterilization Methods#
| Method |
|---|
| Ethylene Oxide |
Regulatory Flags#
- DUNS number
- 070556204
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- false
- HCT/P
- false
- Kit
- true
- Combination product
- false
- Lot or batch
- true
- Serial number
- false
- Manufacturing date on label
- false
- Expiration date on label
- true
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- true
- 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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| 08436020769184 | DOSI-FLOW | LEVENTON SAU | FPA | 2023-09-08 |
| 07613117017422 | Soft-Release-Micro | Ypsomed AG | FPA | 2020-09-15 |
| 07613117017446 | Soft-Release-Micro | Ypsomed AG | FPA | 2020-09-15 |
| 07613117017460 | Soft-Release-Micro | Ypsomed AG | FPA | 2020-09-15 |
| 07613117017484 | Soft-Release-Micro | Ypsomed AG | FPA | 2020-09-15 |
| 07613117017507 | Soft-Release-Micro | Ypsomed AG | FPA | 2020-09-15 |
| 07613117017521 | Soft-Release-Micro | Ypsomed AG | FPA | 2020-09-15 |
| 08498840009338 | VYGON | Vygon Corporation | FPA | 2020-04-21 |
| 08498840009895 | VYGON | Vygon Corporation | FPA | 2020-04-21 |
| 08498840010266 | Churchill Medical Systems | Vygon Corporation | FPA | 2020-04-21 |
| 08498840010372 | Churchill Medical Systems | Vygon Corporation | FPA | 2020-04-21 |
| 08498840010389 | Churchill Medical Systems | Vygon Corporation | FPA | 2020-04-21 |
| 08498840006535 | VYGON | Vygon Corporation | FPA | 2020-03-12 |
| 04038917423892 | Safety-Multifly®-Needle | Sarstedt Aktiengesellschaft & Co.KG | FPA | 2019-12-13 |
| 04038917423724 | Multifly®-Needle | Sarstedt Aktiengesellschaft & Co.KG | FPA | 2019-10-06 |
| 04038917423755 | Multifly®-Needle | Sarstedt Aktiengesellschaft & Co.KG | FPA | 2019-10-06 |
| 04038917423762 | Multifly®-Needle | Sarstedt Aktiengesellschaft & Co.KG | FPA | 2019-10-06 |
| 04038917423779 | Multifly®-Needle | Sarstedt Aktiengesellschaft & Co.KG | FPA | 2019-10-06 |
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| 04038917423793 | Multifly®-Needle | Sarstedt Aktiengesellschaft & Co.KG | FPA | 2019-10-06 |
| 04038917423885 | Safety-Multifly®-Needle | Sarstedt Aktiengesellschaft & Co.KG | FPA | 2019-09-30 |
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