Identity
- Trade Name
- Hummingbird FDA UDI
- Generic Name
- Intracerebral catheter cranial-fixation kit FDA UDI
- Device Name
- IC 40 Cranial Access Kit FDA UDI
- Model / Reference
- CK 40 FDA UDI
- Description
- IC 40 Cranial Access Kit FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00850013266234 FDA UDI
- GMDN Term
- Intracerebral catheter cranial-fixation kit FDA UDI
Classification
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Hummingbird by Irras USA — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | N/A | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Irras USA
Sources (1)
- FDA UDI 0b90fe27-b14e-40ea-80ad-48c19233c2c5 35 fields · synced Jun 1, 2026