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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
Test tube/reservoir cap FDA UDI
Device Name
FB PLUG CAP 13MM BECKMN 500/PK FDA UDI
Model / Reference
5538PL-FH FDA UDI
Description
FB PLUG CAP 13MM BECKMN 500/PK FDA UDI

Identifiers

Catalog Number
23555802 FDA UDI
Primary DI / UDI-DI
00613647009284 FDA UDI
FDA Product Code
LXG FDA UDI
GMDN Term
Test tube/reservoir cap FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2050 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: Test tube/reservoir cap

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 Test tube/reservoir cap.

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 9079ac0a-83b7-4ed1-8868-ed459760bc37 35 fields · synced May 30, 2026