Identity
- Trade Name
- ARROW FDA UDI
- Generic Name
- Epidural/intrathecal anaesthesia set, non-medicated FDA UDI
- Device Name
- SureBlock(TM) Spinal Anesthesia Set FDA UDI
- Model / Reference
- IPN040064 FDA UDI
- Description
- SureBlock(TM) Spinal Anesthesia Set FDA UDI
Identifiers
- Catalog Number
- ASA-22090-S FDA UDI
- Primary DI / UDI-DI
- 00801902074218 FDA UDI
- FDA Product Code
- BSP FDA UDI
- GMDN Term
- Epidural/intrathecal anaesthesia set, non-medicated FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 868.5150 FDA UDI
- Commercial Distribution
- 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
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Length — 9 Centimeter FDA UDI
Category: Epidural/intrathecal anaesthesia set, non-medicated
Arrow by Teleflex Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 | Class II | Pending data |
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Manufacturer
- Manufacturer
- Teleflex Incorporated
Sources (1)
- FDA UDI 1032f03c-1716-4c86-93d1-579a5c9156a4 36 fields · synced Jun 6, 2026