Identity
- Trade Name
- Dabir FDA UDI
- Generic Name
- Freestanding/bed-attached intravenous pole FDA UDI
- Device Name
- Clamp FDA UDI
- Model / Reference
- RD-0789 FDA UDI
- Description
- Clamp FDA UDI
Identifiers
- Catalog Number
- RD-0789 FDA UDI
- Primary DI / UDI-DI
- 00761887003460 FDA UDI
- FDA Product Code
- FOX FDA UDI
- GMDN Term
- Freestanding/bed-attached intravenous pole FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.6990 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Freestanding/bed-attached intravenous pole
Dabir by Pryor Products — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Freestanding/bed-attached intravenous pole.
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- Skytron Streamline system with wide wing — Skytron, LLC · Class I
- Disposable IV Pole — Dynarex Corp. · Class I
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 I | Pending data |
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Manufacturer
- Manufacturer
- Pryor Products
Sources (1)
- FDA UDI 0e8fda32-8d03-4301-a390-46d21373ae55 34 fields · synced May 29, 2026