Identity
- Trade Name
- Rumex FDA UDI
- Generic Name
- Corneal bur manual instrument FDA UDI
- Device Name
- Replacement Burr For Alger Brush, 0.50 mm, Burr only, Length 22 mm. 5 per Box FDA UDI
- Model / Reference
- 16-143B FDA UDI
- Description
- Replacement Burr For Alger Brush, 0.50 mm, Burr only, Length 22 mm. 5 per Box FDA UDI
Identifiers
- Catalog Number
- 16-143B FDA UDI
- Primary DI / UDI-DI
- 00840159903353 FDA UDI
- FDA Product Code
- HOF FDA UDI
- GMDN Term
- Corneal bur manual instrument FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 886.4350 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: Corneal bur manual instrument
Rumex by Rumex International Co. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Rumex — Rumex International Co. · Class I
- Rumex — Rumex International Co. · Class I
- Rumex — Rumex International Co. · Class I
- Rumex — Rumex International Co. · Class I
- Rumex — Rumex International Co. · 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
- Rumex International Co.
Sources (1)
- FDA UDI d8f7900f-45f5-432e-b0d3-d096b0637d29 34 fields · synced Jun 9, 2026