← Back to catalogue

TAPESTRY RC Biointegrative Implant System

FDA UDI

by Embody, Inc.

Identity

Trade Name
TAPESTRY RC Biointegrative Implant System FDA UDI
Generic Name
Arthroscopic surgical procedure kit, non-medicated, single-use FDA UDI
Device Name
Convenience Kit FDA UDI
Model / Reference
TR-2030-A6 FDA UDI
Description
Convenience Kit FDA UDI

Identifiers

Catalog Number
TR-2030-A6 FDA UDI
Primary DI / UDI-DI
00810063820206 FDA UDI
GMDN Term
Arthroscopic surgical procedure kit, non-medicated, single-use FDA UDI

Classification

Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Arthroscopic surgical procedure kit, non-medicated, single-use

TAPESTRY RC Biointegrative Implant System by Embody, Inc. — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Arthroscopic surgical procedure kit, non-medicated, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Embody, Inc.

Sources (1)

  • FDA UDI f1c7ca5a-8b84-47b5-960c-08479d95e609 34 fields · synced May 31, 2026