Identity
- Trade Name
- Snowden-Pencer FDA UDI
- Generic Name
- Endoscopic electrosurgical handpiece/electrode, monopolar, reusable FDA UDI
- Device Name
- RESPOSABLE TITANIUM ENDO-RIGHT ANGLE SUCTION ELECTRODE 5MM, 32CM, 5 PER BOX FDA UDI
- Model / Reference
- 89-7202 FDA UDI
- Description
- RESPOSABLE TITANIUM ENDO-RIGHT ANGLE SUCTION ELECTRODE 5MM, 32CM, 5 PER BOX FDA UDI
Identifiers
- Catalog Number
- 897202 FDA UDI
- Primary DI / UDI-DI
- 10885403278648 FDA UDI
- 510(k) Number
- K930666 FDA UDI
- FDA Product Code
- GEI FDA UDI
- GMDN Term
- Endoscopic electrosurgical handpiece/electrode, monopolar, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4400 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
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
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Endoscopic electrosurgical handpiece/electrode, monopolar, reusable
Snowden-Pencer by Steris Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Endoscopic electrosurgical handpiece/electrode, monopolar, reusable.
- Mediflex Deluxe Laparoscopic Instruments — FLEXBAR MACHINE CORP. · Class II
- Bowel Grasper Inner Shaft — ORANGE SURGICAL INSTRUMENTS, LLC · Class II
- AESCULAP — AESCULAP, INC. · Class II
- Hermann Medizintechnik GmbH — Hermann Medizintechnik GmbH · Class II
- Silex — SILEX MEDICAL, LLC · Class II
- AESCULAP — AESCULAP, INC. · Class II
- Signature — SILEX MEDICAL, LLC · Class II
- Dorsey Grasper Inner Shaft — ORANGE SURGICAL INSTRUMENTS, LLC · Class II
Cleared under the same submission
K930666 also covers:
- Snowden-Pencer — STERIS CORPORATION
- Snowden-Pencer — STERIS CORPORATION
- Snowden-Pencer — STERIS CORPORATION
- Snowden-Pencer — STERIS CORPORATION
- Snowden-Pencer — STERIS CORPORATION
- Snowden-Pencer — STERIS CORPORATION
- Snowden-Pencer — STERIS CORPORATION
- Snowden-Pencer — STERIS CORPORATION
- Snowden-Pencer — STERIS CORPORATION
- Snowden-Pencer — STERIS CORPORATION
- Snowden-Pencer — STERIS CORPORATION
- Snowden-Pencer — STERIS CORPORATION
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
- Steris Corporation
Sources (1)
- FDA UDI bd6cf265-8ff2-456e-828e-bc99171bce2f 36 fields · synced Jun 8, 2026