Identity
- Trade Name
- MySign® S FDA UDI
- Generic Name
- Pulse oximeter FDA UDI
- Device Name
- MySign® S incl. F-3211-12 MySign® FDA FDA UDI
- Model / Reference
- incl. F-3211-12 MySign® FDA FDA UDI
- Description
- MySign® S incl. F-3211-12 MySign® FDA FDA UDI
Identifiers
- Catalog Number
- 1002219 FDA UDI
- Primary DI / UDI-DI
- 04036616010092 FDA UDI
- FDA Product Code
- DQA FDA UDI
- GMDN Term
- Pulse oximeter FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.2700 FDA UDI
- Commercial Distribution
- Not 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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
MR Unsafe FDA UDI
Dimensions & Sizes
- Size
- Height — 42 Millimeter FDA UDILength — 166 Millimeter FDA UDIWidth — 242 Millimeter FDA UDI
MySign® S by Honeywell Healthcare Solutions GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 |
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Manufacturer
- Manufacturer
- Honeywell Healthcare Solutions GmbH
Sources (1)
- FDA UDI 468e9769-beda-4ee4-af82-a7cb106db6dc 38 fields · synced May 30, 2026