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Warm Plate

FDA UDI

Class II (US FDA UDI)

by Reprolife Inc.

Identity

Trade Name
Warm Plate FDA UDI
Generic Name
Tissue cryostorage straw FDA UDI
Device Name
An Individual package we offer contains 10 plates. The package has product label and letters "Warm Plate-10 Plate" are written on it. FDA UDI
Model / Reference
WP010 FDA UDI
Description
An Individual package we offer contains 10 plates. The package has product label and letters "Warm Plate-10 Plate" are written on it. FDA UDI

Identifiers

Primary DI / UDI-DI
04589700010411 FDA UDI
FDA Product Code
PUD FDA UDI
GMDN Term
Tissue cryostorage straw FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.6160 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

Yes

FDA UDI

Category: Tissue cryostorage straw

Warm Plate by Reprolife Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tissue cryostorage straw.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Reprolife Inc.

Sources (1)

  • FDA UDI b2729573-dc4a-4b00-940d-47ccca1711a9 33 fields · synced May 30, 2026