Identity
- Trade Name
- Miller FDA UDI
- Generic Name
- Biliary drain FDA UDI
- Device Name
- Miller Double Mushroom Biliary Stent Set FDA UDI
- Model / Reference
- G03412 FDA UDI
- Description
- Miller Double Mushroom Biliary Stent Set FDA UDI
Identifiers
- Catalog Number
- UBSS-10-5.0-MLR FDA UDI
- Primary DI / UDI-DI
- 00827002034129 FDA UDI
- FDA Product Code
- FGE FDA UDI
- GMDN Term
- Biliary drain FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.5010 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
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
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Biliary drain
Miller by Cook Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Biliary Plastic Stent Set — Micro-Tech (Nanjing) Co., Ltd. · Class II
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 II | Pending data |
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Manufacturer
- Manufacturer
- Cook Incorporated
Sources (1)
- FDA UDI 118da9f6-30c4-42fc-9e63-f4e0235662b7 36 fields · synced Jun 6, 2026