FDA UDI
Not in Commercial Distribution
🇺🇸 United States
DELTAPAQ CERECYTE
DI: 00878528007258
·
Model: CDF100408-30
·
Medos International Sàrl
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1
Basic Information
- Brand Name
- DELTAPAQ CERECYTE
- Primary DI
- 00878528007258
- Version / Model
- CDF100408-30
- Catalog Number
- CDF10040830
- Company Name
- Medos International Sàrl
- Labeler DUNS
- 482661753
- Distribution Status
- Not in Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2015-09-20
- Public Version
- 5
- Public Version Date
- 2023-11-30
- Public Version Status
- Update
- Public Device Record Key
- 6a9ea19d-38c0-4b26-a5ae-8715ae77053d
- Distribution End Date
- 2021-03-30
Device Description
DELTAPAQ microcoil DELTAPAQ 10 CERECYTE Coil 4mm x 8cm 190cm Contents: 1 Detachable Coil System
Device Characteristics
- Single Use
- Yes
- Prescription Use (Rx)
- Yes
- Over the Counter (OTC)
- No
- Kit
- No
- Combination Product
- No
- HCT/P
- No
- Contains NRL
- No
- Not Made with NRL
- No
- MRI Safety
- MR Conditional
- 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 |
|---|---|---|---|---|
| HCG | DEVICE, NEUROVASCULAR EMBOLIZATION | Neurology | 882.5950 | 2 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 60940 | Neurovascular embolization coil | A non-bioabsorbable, implantable device intended to induce a neurovascular thrombosis to treat an intracranial aneurysm and/or neurovascular arteriovenous malformation (AVM); it may also be intended to treat non-neurovascular malformations. It is in the form of a metal [e.g., platinum alloy] or metal/synthetic polymer wire which coils upon deployment within the aneurysm/vasculature; it is typically pre-attached to a nonimplantable delivery wire. Disposable devices associated with implantation (e.g., delivery wire, catheter) may be included. | Yes | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Primary | 00878528007258 | GS1 |
Customer Contacts
- Phone
- +1(800)255-2500
- [email protected]
Premarket Submissions
| Submission Number | Supplement Number |
|---|---|
| K080437 | 000 |
Storage Conditions
- Type
- Special Storage Condition, Specify
- Special Conditions
- Keep Dry
- Type
- Handling Environment Temperature
- Temperature Range
- 0 – 45 Degrees Celsius
- Type
- Storage Environment Temperature
- Temperature Range
- 0 – 45 Degrees Celsius
- Type
- Storage Environment Temperature
- Temperature Range
- 32 – 110 Degrees Fahrenheit
- Type
- Handling Environment Temperature
- Temperature Range
- 32 – 110 Degrees Fahrenheit