Micro Access
- Primary DI
- H787065072015
- Brand
- Micro Access
- Company
- ANGIODYNAMICS, INC.
- Model
- 06507201
- Device description
- Stainless Steel Guidewire
- Published
- 2016-09-20
- 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
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| DQX | WIRE, GUIDE, CATHETER |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| DQX | Wire, Guide, Catheter | Cardiovascular | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K051655 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| H787065072015 | Package | HIBCC | 10 | In Commercial Distribution |
| H787065072010 | Primary | HIBCC | 0 | |
| 15051684012041 | Secondary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized |
|---|---|
| 15051684012041 | 15051684012041 |
GMDN Terms#
| Term | Definition |
|---|---|
| Vascular catheter introduction set, nonimplantable | A collection of sterile, nonimplantable, invasive devices intended to provide percutaneous vascular access to enable introduction of a catheter (not included) into the vascular system. It includes a non-steerable introducer sheath with an inner obturator/dilator, and typically an additional access device(s) [e.g., guidewire, introducer needle, syringe, additional dilators] which may include a haemostatic valve to control blood loss, usually to enable arterial access. This is a single-use device. |
Device Sizes#
| Type | Value | Unit |
|---|---|---|
| Length | 45 | Centimeter |
| Outer Diameter | 0.018 | Inch |
Storage And Handling#
| Type | Low | High | Condition |
|---|---|---|---|
| Storage Environment Temperature | 0 | 27 Degrees Celsius |
Sterilization Methods#
| Method |
|---|
Contacts#
| Phone | |
|---|---|
| +1(518)795-1676 | dgreer@angiodynamics.com |
Regulatory Flags#
- DUNS number
- 079105071
- 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
- true
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- false
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| H787140650 | Syntrax Support Catheter | 14-065 | 2021-11-02 | |
| H787140900 | Syntrax Support Catheter | 14-090 | 2021-11-02 | |
| H787141350 | Syntrax Support Catheter | 14-135 | 2021-11-02 | |
| H787141500 | Syntrax Support Catheter | 14-150 | 2021-11-02 | |
| H787141800 | Syntrax Support Catheter | 14-180 | 2021-11-02 | |
| H787180650 | Syntrax Support Catheter | 18-065 | 2021-11-02 | |
| H787180900 | Syntrax Support Catheter | 18-090 | 2021-11-02 | |
| H787181350 | Syntrax Support Catheter | 18-135 | 2021-11-02 | |
| H787181500 | Syntrax Support Catheter | 18-150 | 2021-11-02 | |
| H787181800 | Syntrax Support Catheter | 18-180 | 2021-12-16 | |
| H787350650 | Syntrax Support Catheter | 35-065 | 2021-11-02 | |
| H787350900 | Syntrax Support Catheter | 35-090 | 2021-11-02 | |
| H787351350 | Syntrax Support Catheter | 35-135 | 2021-11-02 | |
| H787351500 | Syntrax Support Catheter | 35-150 | 2021-11-02 | |
| H787351801 | Syntrax Support Catheter | 35-180 | 2021-11-02 | |
| 15051684018777 | BioFlo | H965440270 | 44-027 | 2024-09-20 |
| 15051684018784 | BioFlo | H965440280 | 44-028 | 2024-09-20 |
| 05051684018473 | Lifeport | H787LPS30040 | LPS3004 | 2026-06-23 |
| 05051684018480 | Lifeport | H787LPS30050 | LPS3005 | 2026-06-23 |
| 05051684018497 | Lifeport | H787LPS30060 | LPS3006 | 2026-06-23 |
Other Devices Sharing Product Codes#
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|---|---|---|---|---|
| 10801902226430 | ARROW | TELEFLEX INCORPORATED | DQX | 2026-08-10 |
| 10801902206241 | ARROW | TELEFLEX INCORPORATED | DQX | 2026-08-03 |
| 10801902192230 | ARROW | TELEFLEX INCORPORATED | DQX | 2026-08-01 |
| 04547327167215 | CROSSLOOP | ASAHI INTECC CO., LTD. | DQX | 2026-07-31 |
| 04547327167222 | CROSSLOOP | ASAHI INTECC CO., LTD. | DQX | 2026-07-31 |
| 04547327167239 | CROSSLOOP | ASAHI INTECC CO., LTD. | DQX | 2026-07-31 |
| 04547327167246 | CROSSLOOP | ASAHI INTECC CO., LTD. | DQX | 2026-07-31 |
| 04547327167253 | CROSSLOOP | ASAHI INTECC CO., LTD. | DQX | 2026-07-31 |
| 04547327167260 | CROSSLOOP | ASAHI INTECC CO., LTD. | DQX | 2026-07-31 |
| 10801902190908 | ARROW | TELEFLEX INCORPORATED | DQX | 2026-07-30 |
| 10801902198461 | ARROW | TELEFLEX INCORPORATED | DQX | 2026-07-30 |
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| 10705032057042 | AQUATRACK™ Hydrophilic Nitinol Guidewire | Cordis US Corp. | DQX | 2026-07-29 |
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| 10705032057066 | AQUATRACK™ Hydrophilic Nitinol Guidewire | Cordis US Corp. | DQX | 2026-07-29 |
| 10705032057073 | AQUATRACK™ Hydrophilic Nitinol Guidewire | Cordis US Corp. | DQX | 2026-07-29 |
| 10705032057080 | AQUATRACK™ Hydrophilic Nitinol Guidewire | Cordis US Corp. | DQX | 2026-07-29 |
| 10801902193237 | ARROW | TELEFLEX INCORPORATED | DQX | 2026-07-29 |
| 10801902193244 | ARROW | TELEFLEX INCORPORATED | DQX | 2026-07-29 |
| 10801902195101 | ARROW | TELEFLEX INCORPORATED | DQX | 2026-07-29 |
| 10801902193251 | ARROW | TELEFLEX INCORPORATED | DQX | 2026-07-27 |
| 10801902193268 | ARROW | TELEFLEX INCORPORATED | DQX | 2026-07-27 |
| 10801902193275 | ARROW | TELEFLEX INCORPORATED | DQX | 2026-07-27 |
| 10801902222357 | ARROW | TELEFLEX INCORPORATED | DQX | 2026-07-27 |
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| 06936733736951 | ULTRASKIN | Lepu Medical Technology (Beijing) Co.,Ltd. | DQX | 2026-07-10 |