← Back to catalogue

Sterrad

FDA UDI

Class I (US FDA UDI)

by Advanced Sterilization Products Services Inc.

Identity

Trade Name
Sterrad FDA UDI
Generic Name
Laboratory thermometer FDA UDI
Device Name
Thermometer FDA UDI
Model / Reference
82-06845-001 FDA UDI
Description
Thermometer FDA UDI

Identifiers

Catalog Number
82-06845-001 FDA UDI
Primary DI / UDI-DI
10705037041657 FDA UDI
FDA Product Code
JTQ FDA UDI
GMDN Term
Laboratory thermometer FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
866.2540 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

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: Laboratory thermometer

Sterrad by Advanced Sterilization Products Services Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Laboratory thermometer.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI d1f54e10-4fec-4f1c-92f0-be576a69b209 36 fields · synced May 30, 2026