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Fisherbrand

FDA UDI

Class I (US FDA UDI)

by Fisher Scientific Company L.l.c.

Identity

Trade Name
Fisherbrand FDA UDI
Generic Name
Urine specimen collection kit IVD FDA UDI
Device Name
URINE COLLECTION SYSTEM 500/CS FDA UDI
Model / Reference
14377251 FDA UDI
Description
URINE COLLECTION SYSTEM 500/CS FDA UDI

Identifiers

Catalog Number
14377251 FDA UDI
Primary DI / UDI-DI
00613647003596 FDA UDI
FDA Product Code
JXA FDA UDI
GMDN Term
Urine specimen collection kit IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
866.2660 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Urine specimen collection kit IVD

Fisherbrand by Fisher Scientific Company L.l.c. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Urine specimen collection kit IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2897e702-8d22-4fa6-bae4-20e3619bb38b 35 fields · synced Jun 8, 2026