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Sterile Specimen Container

FDA UDI

Class I (US FDA UDI)

by Thermo Fisher Scientific (Monterrey), S. de R.L. de C.V.

Identity

Trade Name
Sterile Specimen Container FDA UDI
Generic Name
General specimen container IVD, no additive/medium FDA UDI
Device Name
60ml/48mmSPCw/LBL, GRN CAP, ST FDA UDI
Model / Reference
030008 FDA UDI
Description
60ml/48mmSPCw/LBL, GRN CAP, ST FDA UDI

Identifiers

Primary DI / UDI-DI
17503025060122 FDA UDI
FDA Product Code
FMH FDA UDI
GMDN Term
General specimen container IVD, no additive/medium FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.3250 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

No

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
Sterilization Method
Radiation Sterilization FDA UDI

Sterile Specimen Container by Thermo Fisher Scientific (Monterrey), S. de R.L. de C.V. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 756ed23b-57ac-4ed0-94ca-111526ce78d5 34 fields · synced May 30, 2026