Identity
- Trade Name
- ACCUTRAY FDA UDI
- Generic Name
- Epidural anaesthesia set, non-medicated FDA UDI
- Model / Reference
- 5200113B FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10809160283639 FDA UDI
- FDA Product Code
- OGJ FDA UDI
- GMDN Term
- Epidural anaesthesia set, non-medicated FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 868.5140 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
Yes
FDA UDI
Combination Product
Yes
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
Category: Epidural anaesthesia set, non-medicated
Accutray by Medical Action Industries Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Epidural anaesthesia set, non-medicated.
- Portex — ICU MEDICAL, INC. · Class II
- CARDINAL HEALTH — Cardinal Health 200, LLC · Class II
- ARROW — TELEFLEX INCORPORATED · Class II
- Busse Hospital Disposables — ROBERT BUSSE & CO., INC. · Class II
- CARDINAL HEALTH — Cardinal Health 200, LLC · Class II
- Portex — ICU MEDICAL, INC. · Class II
- DeRoyal — DEROYAL INDUSTRIES, INC. · Class II
- CARDINAL HEALTH — Cardinal Health 200, LLC · Class II
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Medical Action Industries Inc.
Sources (1)
- FDA UDI b8f71817-da6b-4a54-81d7-d02c77444a26 33 fields · synced Jun 6, 2026