Identity
- Trade Name
- Safire™ TX FDA UDI
- Generic Name
- Electrical-only medical device connection cable, reprocessed FDA UDI
- Device Name
- Catheter Extension Cable Stockert Generator 1740-SW FDA UDI
- Model / Reference
- 402579 FDA UDI
- Description
- Catheter Extension Cable Stockert Generator 1740-SW FDA UDI
Identifiers
- Catalog Number
- 402579 FDA UDI
- Primary DI / UDI-DI
- 05414734300261 FDA UDI
- PMA Number
- P040042 FDA UDI
- FDA Product Code
- OAD FDA UDI
- GMDN Term
- Electrical-only medical device connection cable, reprocessed FDA UDI
Classification
- Device Class
- Class III 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
No
FDA UDI
Dimensions & Sizes
- Size
- Length — 2.5 Meter FDA UDI
Category: Electrical-only medical device connection cable, reprocessed
Safire™ TX by Irvine Biomedical, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Electrical-only medical device connection cable, reprocessed.
- Greenwald Surgical Company, Inc. — GRACE MANUFACTURING INC · Class II
- Greenwald Surgical Company, Inc. — GRACE MANUFACTURING INC · Class II
- Greenwald Surgical Company, Inc. — GRACE MANUFACTURING INC · Class II
- Greenwald Surgical Company, Inc. — GRACE MANUFACTURING INC · Class II
- Greenwald Surgical Company, Inc. — GRACE MANUFACTURING INC · Class II
- Medtronic — Stryker Sustainability Solutions · Class II
- Greenwald Surgical Company, Inc. — GRACE MANUFACTURING INC · Class II
- Greenwald Surgical Company, Inc. — GRACE MANUFACTURING INC · Class II
Cleared under the same submission
P040042 also covers:
- Safire™ TX — IRVINE BIOMEDICAL, INC.
- Safire™ TX — IRVINE BIOMEDICAL, INC.
- Safire™ TX — IRVINE BIOMEDICAL, INC.
- Safire™ TX — IRVINE BIOMEDICAL, INC.
- Safire™ TX — IRVINE BIOMEDICAL, INC.
- Safire™ TX — IRVINE BIOMEDICAL, INC.
- Safire™ TX — IRVINE BIOMEDICAL, INC.
- Therapy™ — IRVINE BIOMEDICAL, INC.
- Therapy™ — IRVINE BIOMEDICAL, INC.
- Therapy™ — IRVINE BIOMEDICAL, INC.
- Therapy™ — IRVINE BIOMEDICAL, INC.
- Therapy™ — IRVINE BIOMEDICAL, INC.
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 III | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Irvine Biomedical, Inc.
Sources (1)
- FDA UDI 4c27f0a1-771d-42ca-85df-7cf459764ec1 38 fields · synced Jun 8, 2026