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Integra® PyroCarbon

FDA UDI

Class I (US FDA UDI)

by Ascension Orthopedics, Inc.

Identity

Trade Name
Integra® PyroCarbon FDA UDI
Generic Name
Instrument tray, reusable FDA UDI
Device Name
Pyrocarbon CMC FDA UDI
Model / Reference
PYROSADINSTP FDA UDI
Description
Pyrocarbon CMC FDA UDI

Identifiers

Catalog Number
PYROSADINSTP FDA UDI
Primary DI / UDI-DI
10381780282457 FDA UDI
FDA Product Code
OJH FDA UDI
HWB FDA UDI
HTQ FDA UDI
HWT FDA UDI
HWA FDA UDI
FZX FDA UDI
HWJ FDA UDI
GMDN Term
Instrument tray, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
888.4540 FDA UDI
888.4800 FDA UDI
Commercial Distribution
Not 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

Yes

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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Integra® PyroCarbon by Ascension Orthopedics, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1925022f-d9cd-4471-8499-4d4a73aef9e3 36 fields · synced May 31, 2026