FDA UDI
In Commercial Distribution
🇺🇸 United States
GLIDESHEATH SLENDER
DI: 00389701012001
·
Model: 60-1075
·
TERUMO MEDICAL CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1
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Basic Information
- Brand Name
- GLIDESHEATH SLENDER
- Primary DI
- 00389701012001
- Version / Model
- 60-1075
- Catalog Number
- 60-1075
- Company Name
- TERUMO MEDICAL CORPORATION
- Labeler DUNS
- 131489882
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2018-05-23
- Public Version
- 3
- Public Version Date
- 2024-03-20
- Public Version Status
- Update
- Public Device Record Key
- 6593af8a-9423-47c6-96d0-bd0725aae80f
Device Description
GLIDESHEATH SLENDER Access Kit
Device Characteristics
- Single Use
- Yes
- Prescription Use (Rx)
- No
- Over the Counter (OTC)
- No
- Kit
- Yes
- Combination Product
- No
- HCT/P
- No
- Contains NRL
- No
- Not Made with NRL
- No
- MRI Safety
- Labeling does not contain MRI Safety Information
- Direct Marking Exempt
- No
- PM Exempt
- No
- Has Serial Number
- No
- Has Lot/Batch Number
- Yes
- Has Manufacturing Date
- No
- Has Expiration Date
- Yes
- Has Donation ID
- No
Sterilization
- Is Sterile
- Yes
- Sterilization Prior Use
- No
Product Codes
| Code | Name | Medical Specialty | Regulation # | Device Class |
|---|---|---|---|---|
| DYB | INTRODUCER, CATHETER | Cardiovascular | 870.1340 | 2 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 58865 | Vascular catheter introduction set, nonimplantable | A collection of 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. | No | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Package | 30389701012002 | GS1 | Shelfbox | 5 | In Commercial Distribution | |
| Primary | 00389701012001 | GS1 | ||||
| Package | 50389701012006 | GS1 | Carton | 10 | In Commercial Distribution |
Customer Contacts
- Phone
- +1(800)283-7866
- [email protected]
Device Sizes
| Type | Value | Unit | Text |
|---|---|---|---|
| Device Size Text, specify | Needle: 20 Gauge x 1.259" (32 mm) | ||
| Catheter Gauge | 7 | French | |
| Device Size Text, specify | Guidewire: 0.025 Inch x 45 cm Plastic Jacketed Shortangle | ||
| Length | 10 | Centimeter |
Storage Conditions
- Type
- Special Storage Condition, Specify
- Special Conditions
- Do not store at extreme temperature and humidity
- Type
- Special Storage Condition, Specify
- Special Conditions
- Avoid direct sunlight. Keep Dry.