← Back to catalogue

Marketlab

FDA UDI

Class I (US FDA UDI)

by Marketlab Inc.

Identity

Trade Name
Marketlab FDA UDI
Generic Name
General laboratory container, single-use FDA UDI
Device Name
Easy Open Biohazard Specimen Bags PK1000 FDA UDI
Model / Reference
108165 FDA UDI
Description
Easy Open Biohazard Specimen Bags PK1000 FDA UDI

Identifiers

Primary DI / UDI-DI
00817517026252 FDA UDI
FDA Product Code
NNI FDA UDI
GMDN Term
General laboratory container, single-use 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

No

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Category: General laboratory container, single-use

Marketlab by Marketlab Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General laboratory container, single-use.

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

Manufacturer
Marketlab Inc.

Sources (1)

  • FDA UDI cd550e40-7845-4c2c-90fa-35e414879f40 33 fields · synced May 30, 2026