Identity
- Trade Name
- Garrett Vessel Probe 21cm 1.0mm FDA UDI
- Generic Name
- Vascular dilator, reusable FDA UDI
- Device Name
- Garrett Vessel Probe 21cm 1.0mm FDA UDI
- Model / Reference
- 21-0142 FDA UDI
- Description
- Garrett Vessel Probe 21cm 1.0mm FDA UDI
Identifiers
- Catalog Number
- 21-0142 FDA UDI
- Primary DI / UDI-DI
- 04057034047132 FDA UDI
- FDA Product Code
- DWP FDA UDI
- GMDN Term
- Vascular dilator, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.4475 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
Category: Vascular dilator, reusable
Garrett Vessel Probe 21cm 1.0mm by Geister Medizin Technik GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Geister Medizin Technik GmbH
Sources (1)
- FDA UDI 02d61c4d-c2f0-4232-9451-7923fe5c2fb8 35 fields · synced May 30, 2026