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LLD 129 Basic

FDA UDI

Class I (US FDA UDI)

by Drtech Corp.

Identity

Trade Name
LLD 129 Basic FDA UDI
Generic Name
X-ray film cassette holder FDA UDI
Device Name
The LLD Bucky Stand is combined with the General Xray system, is generally applicable to Xray radiography in Long bone. FDA UDI
Model / Reference
LLD 129 Basic FDA UDI
Description
The LLD Bucky Stand is combined with the General Xray system, is generally applicable to Xray radiography in Long bone. FDA UDI

Identifiers

Primary DI / UDI-DI
08800018421307 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

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: X-ray film cassette holder

LLD 129 Basic by Drtech Corp. — 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
Drtech Corp.

Sources (1)

  • FDA UDI 254a1e46-aba5-413f-9c2a-474015a15d06 33 fields · synced May 30, 2026