Primary Device ID | 15420045516144 |
NIH Device Record Key | a659377c-ad97-44a0-9d5c-0a82b808d2b7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Fluent Pro Procedure Kit |
Version Model Number | FLT-212S |
Catalog Number | FLT-212S |
Company DUNS | 018925968 |
Company Name | Hologic, Inc. |
Device Count | 1 |
DM Exempt | true |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | true |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(800)442-9892 |
CustomerSupport@hologic.com | |
Phone | +1(800)442-9892 |
CustomerSupport@hologic.com | |
Phone | +1(800)442-9892 |
CustomerSupport@hologic.com | |
Phone | +1(800)442-9892 |
CustomerSupport@hologic.com | |
Phone | +1(800)442-9892 |
CustomerSupport@hologic.com | |
Phone | +1(800)442-9892 |
CustomerSupport@hologic.com | |
Phone | +1(800)442-9892 |
CustomerSupport@hologic.com | |
Phone | +1(800)442-9892 |
CustomerSupport@hologic.com | |
Phone | +1(800)442-9892 |
CustomerSupport@hologic.com | |
Phone | +1(800)442-9892 |
CustomerSupport@hologic.com | |
Phone | +1(800)442-9892 |
CustomerSupport@hologic.com | |
Phone | +1(800)442-9892 |
CustomerSupport@hologic.com | |
Phone | +1(800)442-9892 |
CustomerSupport@hologic.com | |
Phone | +1(800)442-9892 |
CustomerSupport@hologic.com | |
Phone | +1(800)442-9892 |
CustomerSupport@hologic.com | |
Phone | +1(800)442-9892 |
CustomerSupport@hologic.com | |
Phone | +1(800)442-9892 |
CustomerSupport@hologic.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 15420045516144 [Primary] |
HIG | Insufflator, hysteroscopic |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-10-23 |
Device Publish Date | 2024-10-15 |
15420045517394 - Hologic | 2025-09-05 NG Res Primers Analyte Specific Reagent. |
15420045517400 - Hologic | 2025-09-05 NG Res Probe (FAM) Analyte Specific Reagent. |
15420045517417 - Hologic | 2025-09-05 NG Res C272T IVT Control (Positive Control). |
15420045517424 - Hologic | 2025-09-05 NG IVT Wild Type Control (Negative Control). |
15420045512412 - DEFINITY CERVICAL DILATOR, 5MM | 2025-07-29 |
15420045512429 - DEFINITY CERVICAL DILATOR, 7MM | 2025-07-29 |
15420045512436 - DEFINITY CERVICAL DILATOR, 9MM | 2025-07-29 |
15420045517097 - DIGITAL DIAGNOSTICS SYSTEM | 2025-07-25 Computer to operate the Genius™ Review Station. |