Identity
- Trade Name
- INSORB FDA UDI
- Generic Name
- Skin stapler/staple, bioabsorbable FDA UDI
- Device Name
- INSORB Subcuticular Skin Stapler REF2030 (each) FDA UDI
- Model / Reference
- 2030 FDA UDI
- Description
- INSORB Subcuticular Skin Stapler REF2030 (each) FDA UDI
Identifiers
- Catalog Number
- REF2030 FDA UDI
- Primary DI / UDI-DI
- 00867516000104 FDA UDI
- FDA Product Code
- GDW FDA UDIQQS FDA UDI
- GMDN Term
- Skin stapler/staple, bioabsorbable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4750 FDA UDI878.4740 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
Category: Skin stapler/staple, bioabsorbable
Insorb by CooperSurgical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- SubQ It! — Opus Ksd, Inc. · Class II
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- CooperSurgical, Inc.
Sources (1)
- FDA UDI 12d5ab9c-2728-4bf2-a556-667fd2c6f1ff 35 fields · synced Jun 9, 2026