Identity
- Trade Name
- Henry Schein FDA UDI
- Generic Name
- Electrosurgical system FDA UDI
- Device Name
- H-Type Sharp Tip Disposable FDA UDI
- Model / Reference
- 5700890 FDA UDI
- Description
- H-Type Sharp Tip Disposable FDA UDI
Identifiers
- Catalog Number
- 5700890 FDA UDI
- Primary DI / UDI-DI
- 10304040071004 FDA UDI
- FDA Product Code
- HGI FDA UDI
- GMDN Term
- Electrosurgical system 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
No
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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Electrosurgical system
Henry Schein by Henry Schein, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Electrosurgical system.
- Bovie — BOVIE MEDICAL CORPORATION · Class II
- Macan — Macan Manufacturing · Class II
- Macan — Macan Manufacturing · Class II
- T4 Fine wire electrode — BONART CO., LTD. · Class II
- DIEGO ELITE — Gyrus Acmi, Inc. · Class II
- Macan — Macan Manufacturing · Class II
- DeRoyal — DEROYAL INDUSTRIES, INC. · Class II
- Bovie — BOVIE MEDICAL CORPORATION · 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Henry Schein, Inc.
Sources (1)
- FDA UDI ef5777a2-d398-4515-b6e1-43feff1e5074 34 fields · synced Jun 8, 2026