← Back to catalogue
Cannula for subcutaneous Implant/ pellet administration
FDA UDIClass I (US FDA UDI)
Identity
- Trade Name
- Cannula for subcutaneous Implant/ pellet administration FDA UDI
- Generic Name
- Pellet implantation cannula, single-use FDA UDI
- Device Name
- Cannula for subcutaneous Implant/ pellet administration, 14 G x 50mm FDA UDI
- Model / Reference
- 10000 FDA UDI
- Description
- Cannula for subcutaneous Implant/ pellet administration, 14 G x 50mm FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04063574100008 FDA UDI
- FDA Product Code
- GEA FDA UDI
- GMDN Term
- Pellet implantation cannula, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 FDA UDI
- 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
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
MR Unsafe FDA UDI
Category: Pellet implantation cannula, single-use
Cannula for subcutaneous Implant/ pellet administration by sfm medical devices GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Pellet implantation cannula, single-use.
- Doctor Nice — B. Ali Impex · Class II
- Stradis Medical, LLC — STRADIS MEDICAL, LLC · Class II
- Sterling Medical Products — APOLLO MEDICAL PRODUCTS CORP.
- Sterling Medical Products — APOLLO MEDICAL PRODUCTS CORP.
- Sterling Medical Products — APOLLO MEDICAL PRODUCTS CORP.
- Doctor Nice — B. Ali Impex · Class II
- Sterling Medical Products — APOLLO MEDICAL PRODUCTS CORP.
- Sterling Medical Products — APOLLO MEDICAL PRODUCTS CORP.
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
- sfm medical devices GmbH
Sources (1)
- FDA UDI 1670c17a-8d5f-4aa3-865a-03984926c731 33 fields · synced May 30, 2026