Identity
- Trade Name
- Rumex FDA UDI
- Generic Name
- Surgical irrigation/aspiration handpiece, reusable FDA UDI
- Device Name
- Aspiration Handpiece For Bimanual Technique, Curved, 23 Ga, One Top Port 0.30 mm, Length 104 mm, Titanium Handle FDA UDI
- Model / Reference
- 7-0821-23 FDA UDI
- Description
- Aspiration Handpiece For Bimanual Technique, Curved, 23 Ga, One Top Port 0.30 mm, Length 104 mm, Titanium Handle FDA UDI
Identifiers
- Catalog Number
- 7-0821-23 FDA UDI
- Primary DI / UDI-DI
- 00840159900048 FDA UDI
- FDA Product Code
- KYG FDA UDI
- GMDN Term
- Surgical irrigation/aspiration handpiece, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 886.4360 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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Surgical irrigation/aspiration handpiece, reusable
Rumex by Rumex International Co. — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- Rumex International Co.
Sources (1)
- FDA UDI fb4925ef-9c58-4da3-9744-cd8f8d8b47c7 34 fields · synced Jun 9, 2026