Identity
- Trade Name
- ASP MEDICAL FDA UDI
- Generic Name
- Skin staple remover, single-use FDA UDI
- Device Name
- REMOVER SKIN STAPLER EACHES PER CASE 200, 1/EA,200/CS FDA UDI
- Model / Reference
- SGT401 FDA UDI
- Description
- REMOVER SKIN STAPLER EACHES PER CASE 200, 1/EA,200/CS FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00840216104372 FDA UDI
- FDA Product Code
- GDT FDA UDI
- GMDN Term
- Skin staple remover, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4760 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
Yes
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
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Ethylene Oxide FDA UDI
Asp Medical by Asp Global, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Asp Global, LLC
Sources (1)
- FDA UDI 992d9b07-24e2-42bb-a7d8-776f17c971c5 34 fields · synced Jun 1, 2026