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
30382904433766
GS1
June 05, 2025
100
122561087 *Terms of Use
BD MAX UVE Specimen Collection Kit
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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
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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
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FDA Premarket Submission

FDA Premarket Submission Number [?] Supplement Number [?]
K151589 000
No CLOSE

Sterilization

No
No
Sterilization Method [?]
No Sterilization Methods Found
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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
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Clinically Relevant Size

[?]
Size Type Text
No Device Sizes
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Device Record Status

8ea93389-6307-4900-909d-7ca3064ed18b
June 06, 2025
7
October 17, 2016
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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
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Secondary DI

[?]
Issuing Agency [?] Secondary DI Number
No Secondary DIs found
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Unit of Use DI

[?]
Unit of Use DI Number: 00382904433765 CLOSE

Direct Marking (DM)

[?]
No
No
None
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Production Identifier(s) in UDI

[?]
Yes
No
Yes
No
No CLOSE

Customer Contact

[?]
+1(800)638-8663
Technical_services@bd.com
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