Medline DYNJAATREE1
Medline DYNJAATREE1 is a Class I device made by Medline Industries, Inc., listed in FDA GUDID since 27 Mar 2024 (UDI-DI 40080196150091), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number40080196150091 | Date27 Mar 2024 | StatusListed |
Official records
- AccessGUDID record 40080196150091
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Medline
- Generic name
- Breathing circuit tube holder
- Model / Ref / Catalog
- DYNJAATREE1
- Primary DI / UDI-DI
- 40080196150091
- FDA product code
- JAY
- GMDN term
- Breathing circuit tube holder
- Device class
- Class I
- Regulation number
- 868.5280
- GUDID distribution status
- In Commercial Distribution
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