Identity
- Trade Name
- 5560 7L SYRINGE FDA UDI
- Generic Name
- Spirometer/pulmonary function analyser syringe FDA UDI
- Device Name
- REGULATOR CGA973 3KPSI 10MMOD FDA UDI
- Model / Reference
- 5560 FDA UDI
- Description
- REGULATOR CGA973 3KPSI 10MMOD FDA UDI
Identifiers
- Catalog Number
- 171149 FDA UDI
- Primary DI / UDI-DI
- 00817136023755 FDA UDI
- FDA Product Code
- BXW FDA UDI
- GMDN Term
- Spirometer/pulmonary function analyser syringe FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 868.1870 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
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
5560 7l Syringe by Hans Rudolph, Inc. — Class I — 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 I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Hans Rudolph, Inc.
Sources (1)
- FDA UDI 1b3ad988-f73e-41bd-9fe5-a648e3eff260 35 fields · synced Jun 8, 2026