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Montage CT 7cc

FDA UDI

Class U (US FDA UDI)

by Abyrx, Inc.

Identity

Trade Name
Montage CT 7cc FDA UDI
Generic Name
Bone wax, synthetic FDA UDI
Model / Reference
OS-MON-1401CT FDA UDI

Identifiers

Primary DI / UDI-DI
00850391007436 FDA UDI
FDA Product Code
MTJ FDA UDI
GMDN Term
Bone wax, synthetic FDA UDI

Classification

Device Class
U FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Bone wax, synthetic

Montage CT 7cc by Abyrx, Inc. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone wax, synthetic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Abyrx, Inc.

Sources (1)

  • FDA UDI b8e95f77-2895-4898-b670-4585f24481bc 32 fields · synced May 29, 2026