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Phosphor Plate Barrier Envelopes

FDA UDI

Class II (US FDA UDI)

by Maxill, Inc.

Identity

Trade Name
PHOSPHOR PLATE BARRIER ENVELOPES FDA UDI
Generic Name
Digital imaging cassette FDA UDI
Model / Reference
6070553367 FDA UDI

Identifiers

Primary DI / UDI-DI
D89260705533672 FDA UDI
510(k) Number
K163447 FDA UDI
FDA Product Code
PEM FDA UDI
GMDN Term
Digital imaging cassette FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4370 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Digital imaging cassette

Phosphor Plate Barrier Envelopes by Maxill, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Digital imaging cassette.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Maxill, Inc.

Sources (1)

  • FDA UDI 1a5135c8-3ff4-4b38-829e-4cc09b7a3d6c 33 fields · synced May 30, 2026