Identity
- Trade Name
- MiSeal FDA UDI
- Generic Name
- Electrosurgical handpiece, reusable FDA UDI
- Device Name
- MiSeal Handpiece, 14cm, Reusable FDA UDI
- Model / Reference
- 152-101R FDA UDI
- Description
- MiSeal Handpiece, 14cm, Reusable FDA UDI
Identifiers
- Catalog Number
- 152-101R FDA UDI
- Primary DI / UDI-DI
- 00811099011613 FDA UDI
- FDA Product Code
- GEI FDA UDI
- GMDN Term
- Electrosurgical handpiece, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4400 FDA UDI
- Commercial Distribution
- Not 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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
MiSeal by Microline Surgical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Microline Surgical, Inc.
Sources (1)
- FDA UDI 6bcce577-e52c-41fc-afd8-309a989ac0f0 35 fields · synced Jun 6, 2026