Identity
- Trade Name
- Rumex FDA UDI
- Generic Name
- Eye spud/needle FDA UDI
- Device Name
- Davis Foreign Body Spud, Length 130 mm, Round Titanium Handle FDA UDI
- Model / Reference
- 16-153 FDA UDI
- Description
- Davis Foreign Body Spud, Length 130 mm, Round Titanium Handle FDA UDI
Identifiers
- Catalog Number
- 16-153 FDA UDI
- Primary DI / UDI-DI
- 00840159905586 FDA UDI
- FDA Product Code
- HNA FDA UDI
- GMDN Term
- Eye spud/needle 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: Eye spud/needle
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 491afef7-c2f9-4184-9bae-95d13d10561a 34 fields · synced Jun 9, 2026