Identity
- Trade Name
- Snowden-Pencer FDA UDI
- Generic Name
- Rigid endoscope obturator FDA UDI
- Device Name
- THORA-PORT CANNULA AND OBTURATOR 5.5MM DIAMETER, 1.5CM LONG FDA UDI
- Model / Reference
- 88-9120 FDA UDI
- Description
- THORA-PORT CANNULA AND OBTURATOR 5.5MM DIAMETER, 1.5CM LONG FDA UDI
Identifiers
- Catalog Number
- 889120 FDA UDI
- Primary DI / UDI-DI
- 10885403154621 FDA UDI
- 510(k) Number
- K930667 FDA UDI
- FDA Product Code
- GCJ FDA UDI
- GMDN Term
- Rigid endoscope obturator FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.1500 FDA UDI
- Commercial Distribution
- 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
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Rigid endoscope obturator
Snowden-Pencer by Steris Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Rigid endoscope obturator.
- Arthroscopy bridge — SOPRO-COMEG GmbH · Class II
- Biportal Laminoscope, ocular — Joimax GmbH · Class IIa
- TAUT — TELEFLEX INCORPORATED · Class II
- Hysteroscopy obturator — SOPRO-COMEG GmbH · Class II
- Spinal surgery spongiosa pushers — Richard Wolf GmbH · Class I
- USA Elite — Gyrus Acmi, Inc. · Class II
- Trabecular Metal® — Zimmer, Inc. · Class I
- SHARK — Richard Wolf GmbH · Class II
Cleared under the same submission
K930667 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 dfcd925e-0aaf-4799-8674-7ee18c5d8634 36 fields · synced Jun 8, 2026