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HERizon Disposable Endoscopic Forceps - Inverted Tooth
FDA UDIClass I (US FDA UDI)
Identity
- Trade Name
- HERizon Disposable Endoscopic Forceps - Inverted Tooth FDA UDI
- Generic Name
- Rigid endoscopic biopsy forceps, single-use FDA UDI
- Device Name
- Disposable Endoscopic Forceps - Inverted Tooth FDA UDI
- Model / Reference
- JY-DC-350-18-S FDA UDI
- Description
- Disposable Endoscopic Forceps - Inverted Tooth FDA UDI
Identifiers
- Catalog Number
- JY-DC-350-18-S FDA UDI
- Primary DI / UDI-DI
- 00850033976304 FDA UDI
- FDA Product Code
- HFB FDA UDI
- GMDN Term
- Rigid endoscopic biopsy forceps, single-use 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
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
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: Rigid endoscopic biopsy forceps, single-use
HERizon Disposable Endoscopic Forceps - Inverted Tooth by Minerva Surgical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Rigid endoscopic biopsy forceps, single-use.
- THD BIOPSY — THD SPA · Class I
- LiNA OperaScope™ Biopsy Forceps — Lina Medical ApS · Class I
- REDPINE — Guangzhou Red Pine Medical Instrument Co., Ltd. · Class I
- OptiBite Disposable Biopsy Forceps — Micro-Tech (Nanjing) Co., Ltd. · Class I
- EVONOS — Gyrus Acmi, Inc. · Class I
- OptiBite Disposable Biopsy Forceps — Micro-Tech (Nanjing) Co., Ltd. · Class I
- OptiBite Disposable Biopsy Forceps — Micro-Tech (Nanjing) Co., Ltd. · Class I
- THD BIOPSY — THD SPA · Class I
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
- Minerva Surgical, Inc.
Sources (1)
- FDA UDI 878a8116-9650-48a1-9f00-6636b5dfbb5c 36 fields · synced Jun 1, 2026