Identity
- Trade Name
- BOVIE FDA UDI
- Generic Name
- Endoscopic electrosurgical electrode, monopolar, single-use FDA UDI
- Device Name
- MODIFIED BLADE ELECTRODE 2.75'' (6.985CM) 0.01525"' (0.039 CM) FDA UDI
- Model / Reference
- ES37 FDA UDI
- Description
- MODIFIED BLADE ELECTRODE 2.75'' (6.985CM) 0.01525"' (0.039 CM) FDA UDI
Identifiers
- Catalog Number
- ES37 FDA UDI
- Primary DI / UDI-DI
- 00607151056377 FDA UDI
- FDA Product Code
- HGI FDA UDI
- GMDN Term
- Endoscopic electrosurgical electrode, monopolar, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 884.4120 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
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
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Endoscopic electrosurgical electrode, monopolar, single-use
Bovie by Bovie Medical Corporation — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Bovie Medical Corporation
Sources (1)
- FDA UDI 78d24f71-04bd-439b-acf0-fecbbb7a8942 34 fields · synced May 30, 2026