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flora

FDA UDI

Class I (US FDA UDI)

by Core Labs, Llc.

Identity

Trade Name
flora FDA UDI
Generic Name
X-ray film cassette holder FDA UDI
Device Name
Radiographic Wall Cassette Holder XDTG FDA UDI
Model / Reference
08000 FDA UDI
Description
Radiographic Wall Cassette Holder XDTG FDA UDI

Identifiers

Catalog Number
08000 FDA UDI
Primary DI / UDI-DI
00863897000368 FDA UDI
FDA Product Code
IXY FDA UDI
GMDN Term
X-ray film cassette holder FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
892.1880 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

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: X-ray film cassette holder

flora by Core Labs, Llc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as X-ray film cassette holder.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Core Labs, Llc.

Sources (1)

  • FDA UDI 90c3ac08-cc9f-48a5-b5f7-922afaad240b 35 fields · synced May 30, 2026