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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 catalase IVD, kit, rapid colorimetric, clinical FDA UDI
Device Name
URINE RGNT STRIP 10SG 100/PK FDA UDI
Model / Reference
51100 FDA UDI
Description
URINE RGNT STRIP 10SG 100/PK FDA UDI

Identifiers

Catalog Number
23111262 FDA UDI
Primary DI / UDI-DI
00613647008850 FDA UDI
FDA Product Code
CDM FDA UDI
GMDN Term
Urine catalase IVD, kit, rapid colorimetric, clinical FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1785 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

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Urine catalase IVD, kit, rapid colorimetric, clinical

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 catalase IVD, kit, rapid colorimetric, clinical.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2d227938-3f74-4a7b-83a9-c77eda834a0d 35 fields · synced May 29, 2026