Identity
- Trade Name
- Teledyne Analytical Instruments FDA UDI
- Generic Name
- Respiratory oxygen sensor FDA UDI
- Device Name
- Oxygen Sensor FDA UDI
- Model / Reference
- R17MED FDA UDI
- Description
- Oxygen Sensor FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00852470008037 FDA UDI
- 510(k) Number
- K001095 FDA UDI
- FDA Product Code
- CCL FDA UDI
- GMDN Term
- Respiratory oxygen sensor FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 868.1720 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
No
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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Respiratory oxygen sensor
Teledyne Analytical Instruments by Teledyne Analytical Instrs — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Respiratory oxygen sensor.
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- MAX-13 SENSOR, PRECISION MEDICAL 504877 — Maxtec, Inc. · Class II
- Vapotherm — Vapotherm Inc.
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Cleared under the same submission
K001095 also covers:
- Teledyne — Teledyne Analytical Instrs
- Teledyne — Teledyne Analytical Instrs
- Teledyne — Teledyne Analytical Instrs
- Teledyne Analytical Instruments — Teledyne Analytical Instrs
- Teledyne Analytical Instruments — Teledyne Analytical Instrs
- Teledyne Analytical Instruments — Teledyne Analytical Instrs
- Teledyne Analytical Instruments — Teledyne Analytical Instrs
- Teledyne Analytical Instruments — Teledyne Analytical Instrs
- Teledyne Analytical Instruments — Teledyne Analytical Instrs
- Teledyne Analytical Instruments — Teledyne Analytical Instrs
- Teledyne Analytical Instruments — Teledyne Analytical Instrs
- Teledyne Analytical Instruments — Teledyne Analytical Instrs
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
- Teledyne Analytical Instrs
Sources (1)
- FDA UDI 920ec364-4226-44f5-8c1f-d4c010a7205f 34 fields · synced May 30, 2026