← Back to catalogue

Insert, 24 Well, PET 0.4µm, TP

FDA UDI

Class I (US FDA UDI)

by Sarstedt Aktiengesellschaft & Co.KG

Identity

Trade Name
Insert, 24 Well, PET 0.4µm, TP FDA UDI
Generic Name
Tissue culture/microbiology petri dish, single-use FDA UDI
Model / Reference
83.3932.041 FDA UDI

Identifiers

Catalog Number
83.3932.041 FDA UDI
Primary DI / UDI-DI
04038917371346 FDA UDI
FDA Product Code
KIZ FDA UDI
GMDN Term
Tissue culture/microbiology petri dish, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.2240 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Tissue culture/microbiology petri dish, single-use

Insert, 24 Well, PET 0.4µm, TP by Sarstedt Aktiengesellschaft & Co.KG — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tissue culture/microbiology petri dish, 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

Sources (1)

  • FDA UDI 8d5f0e44-87d4-4830-a76c-69873e6d7d56 34 fields · synced May 30, 2026