FDA UDI
In Commercial Distribution
🇺🇸 United States
Adherus AutoSpray ET Dural Sealant
DI: 00897146002025
·
Model: NUS-109
·
HYPERBRANCH MEDICAL TECHNOLOGY, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1
Basic Information
- Brand Name
- Adherus AutoSpray ET Dural Sealant
- Primary DI
- 00897146002025
- Version / Model
- NUS-109
- Company Name
- HYPERBRANCH MEDICAL TECHNOLOGY, INC.
- Labeler DUNS
- 145235953
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2016-12-19
- Public Version
- 4
- Public Version Date
- 2020-04-03
- Public Version Status
- Update
- Public Device Record Key
- 3b888f91-e9ea-499e-9b77-8295d9c41187
Device Description
Adherus AutoSpray Extended Tip (ET) Dural Sealant is a sterile, single-use, electromechanical, battery operated device with internal system components that provide air flow to aid in the delivery of a synthetic, absorbable, two-component hydrogel sealant system and allow delivery to be interrupted without clogging.
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
- 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 |
|---|---|---|---|---|
| NQR | Sealant, Dural | Unknown | 3 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 47171 | Dura mater sealant | An implanted bioabsorbable material (e.g., solution, gel, spray, patch) intended to be applied to a defect in the dura mater, possibly as an adjunct to standard methods of closure (e.g., suturing), to prevent cerebrospinal fluid (CSF) leakage during healing. The material primarily consists of synthetic polymers that subsequently form adhesive bonds with the dura mater and eventually degrade and are absorbed. After application, this device cannot be reused. | Yes | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Package | 30897146002026 | GS1 | 5 | In Commercial Distribution | ||
| Primary | 00897146002025 | GS1 |
Customer Contacts
- Phone
- 9194333332
- [email protected]
Premarket Submissions
| Submission Number | Supplement Number |
|---|---|
| P130014 | 002 |
Storage Conditions
- Type
- Storage Environment Temperature
- Temperature Range
- – 30 Degrees Celsius