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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
Microscopy mounting medium IVD FDA UDI
Device Name
PROTOCOL MOUNTNG MED 16OZ FDA UDI
Model / Reference
11002235 FDA UDI
Description
PROTOCOL MOUNTNG MED 16OZ FDA UDI

Identifiers

Catalog Number
11002235 FDA UDI
Primary DI / UDI-DI
00613647028650 FDA UDI
FDA Product Code
LEB FDA UDI
GMDN Term
Microscopy mounting medium IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.4010 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Microscopy mounting medium 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 Microscopy mounting medium IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Fisher Scientific Company L.l.c.

Sources (1)

  • FDA UDI 019589ae-20a9-4ed2-af93-642d365c7601 35 fields · synced May 30, 2026