Qumulate 3.1
by Varian Medical Systems, Inc.
Qumulate 3.1 is a Class I device made by Varian Medical Systems, Inc., listed in FDA GUDID since 10 Jun 2022 (UDI-DI 00856100006202), registry data as of 8 Nov 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00856100006202 | Date10 Jun 2022 | StatusListed |
Official records
- AccessGUDID record 00856100006202
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Qumulate
- Generic name
- Accelerator system quality assurance device
- Model / reference
- 3.1
- Primary DI / UDI-DI
- 00856100006202
- FDA product code
- OUG
- GMDN term
- Accelerator system quality assurance device
- Device class
- Class I
- Regulation number
- 880.6310
- GUDID distribution status
- In Commercial Distribution
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