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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
Oral/respiratory tract specimen container IVD, no additive/medium FDA UDI
Device Name
SPUTUM KT ST W/50ML TUBE 72/CS FDA UDI
Model / Reference
C200BFS FDA UDI
Description
SPUTUM KT ST W/50ML TUBE 72/CS FDA UDI

Identifiers

Catalog Number
254206 FDA UDI
Primary DI / UDI-DI
00613647023785 FDA UDI
FDA Product Code
FMH FDA UDI
GMDN Term
Oral/respiratory tract specimen container IVD, no additive/medium FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.3250 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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: Oral/respiratory tract specimen container IVD, no additive/medium

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 Oral/respiratory tract specimen container IVD, no additive/medium.

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 696cb02f-e875-4589-879d-7de2ae2b3c78 35 fields · synced Jun 8, 2026