Identity
- Trade Name
- Integra® Miltex® FDA UDI
- Generic Name
- Intrauterine curette, manual FDA UDI
- Device Name
- Integra® Miltex® Greene Uterine Curette 11-1/2", Size 4, 23mm x 13mm Loop, Serrated Blunt Blade, Malleable Shaft FDA UDI
- Model / Reference
- 30-1255-4 FDA UDI
- Description
- Integra® Miltex® Greene Uterine Curette 11-1/2", Size 4, 23mm x 13mm Loop, Serrated Blunt Blade, Malleable Shaft FDA UDI
Identifiers
- Catalog Number
- 30-1255-4 FDA UDI
- Primary DI / UDI-DI
- 10381780442189 FDA UDI
- FDA Product Code
- HCY FDA UDI
- GMDN Term
- Intrauterine curette, manual FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 884.4530 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
Yes
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
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Intrauterine curette, manual
Integra® Miltex® by Integra LifeSciences Production Corporation — 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
- Integra LifeSciences Production Corporation
Sources (1)
- FDA UDI 5cb21cb7-0e91-4977-9a46-3a40ddd40482 35 fields · synced Jun 9, 2026