← Back to catalogue

TissuGlu Surgical Adhesive

FDA UDI

Class III (US FDA UDI)

by Cohera Medical, Inc.

Identity

Trade Name
TissuGlu Surgical Adhesive FDA UDI
Generic Name
Surgical internal adhesive/sealant, synthetic polymer FDA UDI
Device Name
TissuGlu Surgical Adhesive FDA UDI
Model / Reference
TG100US FDA UDI
Description
TissuGlu Surgical Adhesive FDA UDI

Identifiers

Catalog Number
TG100US FDA UDI
Primary DI / UDI-DI
M690TG100US0 FDA UDI
PMA Number
P130023 FDA UDI
FDA Product Code
PJK FDA UDI
GMDN Term
Surgical internal adhesive/sealant, synthetic polymer FDA UDI

Classification

Device Class
Class III FDA UDI
Regulation Number
878.4010 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Radiation Sterilization FDA UDI

Category: Surgical internal adhesive/sealant, synthetic polymer

TissuGlu Surgical Adhesive by Cohera Medical, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical internal adhesive/sealant, synthetic polymer.

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
Cohera Medical, Inc.

Sources (1)

  • FDA UDI 4107c303-e8ab-49ab-a166-cb56071ffc75 37 fields · synced Jun 8, 2026