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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
Tissue embedding mould IVD, single-use FDA UDI
Device Name
FB MICROSTTE NO DIV WHT 250/PK FDA UDI
Model / Reference
M502-2FS FDA UDI
Description
FB MICROSTTE NO DIV WHT 250/PK FDA UDI

Identifiers

Catalog Number
15182706A FDA UDI
Primary DI / UDI-DI
00613647024164 FDA UDI
FDA Product Code
IDZ FDA UDI
GMDN Term
Tissue embedding mould IVD, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.3010 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Tissue embedding mould IVD, single-use

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 Tissue embedding mould IVD, single-use.

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 d2731fbe-aeb3-4da8-b869-2a8901e52dc2 35 fields · synced Jun 6, 2026