DEVICE: BD MAX™ UVE Specimen Collection Kit (30382904433766)
Device Identifier (DI) Information
BD MAX™ UVE Specimen Collection Kit
443376
Not in Commercial Distribution
443376
BECTON, DICKINSON AND COMPANY
443376
Not in Commercial Distribution
443376
BECTON, DICKINSON AND COMPANY
BD MAX UVE Specimen Collection Kit
Device Characteristics
Labeling does not contain MRI Safety Information | |
No | |
No | |
Yes | |
Yes | |
No | |
No | |
No | |
No |
GMDN
[?]GMDN© Term Code, Names and Definitions (*Terms of Use): GMDN® is a registered trademark of The GMDN Agency. All rights reserved. Used under licence from The GMDN Agency Ltd.
GMDN Term Code | GMDN Term Name | GMDN Term Definition | GMDN Term Status [?] | Implantable? |
---|---|---|---|---|
57937 | Urogenital specimen collection kit IVD, clinical |
A collection of devices intended exclusively for professional use for the collection, and preservation and/or transport, of cellular and/or other material collected from the endocervix, vagina, and other male/female lower urogenital area (e.g., urethra) for in vitro diagnostic investigation [e.g., microbiological culture, histopathological cervical cancer screening]. The kit consists of a specimen sampling/collection tool(s) [e.g., swab, brush, spatula], and a covered receptacle with or without an additive/medium (e.g., preservative solution, Amies/Stuart transport medium); initial preparation/fixation/preservation materials may also be included in the kit. This is a single-use device.
|
Active | false |
61144 | Sexually transmitted infection (STI) testing specimen collection kit IVD, clinical |
A collection of devices intended exclusively for professional use to collect a clinical specimen at the point-of-care for subsequent in vitro diagnostic investigation of sexually transmitted infections (STI) [e.g., Chlamydia trachomatis, Neisseria gonorrhoeae, Trichomonas vaginalis, syphilis and human immunodeficiency virus (HIV)]. It consists of one or multiple transport containers, with or without an additive/medium [e.g., preservative solution, microbiological medium (e.g., Amies, Stuart, anaerobic, viral transport/inactivation medium)], and sampling/collection tool(s) [e.g., vaginal, rectal or oropharyngeal swab, brush, spatula, lancet, pipette]. This is a single-use device.
|
Active | false |
FDA Product Code
[?]Product Code | Product Code Name |
---|---|
OUY | Trichomonas vaginalis nucleic acid amplification test system |
MKZ | DNA PROBE, NUCLEIC ACID AMPLIFICATION, CHLAMYDIA |
LSL | DNA-REAGENTS, NEISSERIA |
FDA Premarket Submission
FDA Premarket Submission Number [?] | Supplement Number [?] |
---|---|
K151589 | 000 |
Sterilization
Storage and Handling
[?]Storage and Handling |
---|
Special Storage Condition, Specify: Fragile, handle with care |
Storage Environment Temperature: between 2 and 25 Degrees Celsius |
Special Storage Condition, Specify: This way up |
Special Storage Condition, Specify: Peel here |
Clinically Relevant Size
[?]Size Type Text |
---|
No Device Sizes |
Device Record Status
8ea93389-6307-4900-909d-7ca3064ed18b
June 06, 2025
7
October 17, 2016
June 06, 2025
7
October 17, 2016
Alternative and Additional Identifiers Additional Identifiers
Package DI
[?]Package DI Number | Quantity per Package | Contains DI Package | Package Discontinue Date | Package Status | Package Type |
---|---|---|---|---|---|
No Package DIs found |
Secondary DI
[?]Issuing Agency [?] | Secondary DI Number |
---|---|
No Secondary DIs found |
Unit of Use DI
[?]
Unit of Use DI Number:
00382904433765
CLOSE
Direct Marking (DM)
[?]Production Identifier(s) in UDI
[?]Customer Contact
[?]
+1(800)638-8663
Technical_services@bd.com
Technical_services@bd.com