Globe Scientific 3012B
Globe Scientific 3012B is a microbial cryotube IVD (FDA Class I; FDA product code KDT, Container, Specimen Mailer And Storage, Sterile) made by Globe Scientific, LLC, listed in FDA GUDID since 5 Jul 2023 (UDI-DI 00840095646253), 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 | Number00840095646253 | Date5 Jul 2023 | StatusListed |
Official records
- AccessGUDID record 00840095646253
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Globe Scientific
- Generic name
- Microbial cryotube IVD
- Model / reference
- 3012B
- Primary DI / UDI-DI
- 00840095646253
- FDA product code
- KDT
- GMDN term
- Microbial cryotube IVD
- Device class
- Class I
- Regulation number
- 864.3250
- GUDID distribution status
- In Commercial Distribution
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