Identity
- Trade Name
- EFH-30 FDA UDI
- Generic Name
- Implantable electrical stimulation lead suture sleeve FDA UDI
- Model / Reference
- 119964 FDA UDI
Identifiers
- Catalog Number
- 119964 FDA UDI
- Primary DI / UDI-DI
- 04035479144890 FDA UDI
- PMA Number
- P980023 FDA UDI
- FDA Product Code
- DTB FDA UDI
- GMDN Term
- Implantable electrical stimulation lead suture sleeve FDA UDI
Classification
- Device Class
- Class III FDA UDI
- Regulation Number
- 870.3680 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: Implantable electrical stimulation lead suture sleeve
Efh-30 by BIOTRONIK SE & Co. KG — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Implantable electrical stimulation lead suture sleeve.
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- LS14B20 — Oscor Inc. · Class III
- Ligature Sleeve — Oscor Inc. · Class III
- SJM™ — ST. JUDE MEDICAL, INC. · Class III
- Ligature Sleeve — Oscor Inc. · Class III
Cleared under the same submission
P980023 also covers:
- BK-IS4/DF4 — BIOTRONIK SE & Co. KG
- BS DF-1 — BIOTRONIK SE & Co. KG
- D2-Kit — BIOTRONIK SE & Co. KG
- D2-Kit — BIOTRONIK SE & Co. KG
- D2-Kit — BIOTRONIK SE & Co. KG
- DH DF4 — BIOTRONIK SE & Co. KG
- IS1-C5PS — BIOTRONIK SE & Co. KG
- IS4/DF4 Adapter — BIOTRONIK SE & Co. KG
- IS4/DF4 Adapter — BIOTRONIK SE & Co. KG
- PA 10 — BIOTRONIK SE & Co. KG
- PA-2 — BIOTRONIK SE & Co. KG
- Pamira S DX 65/15 — BIOTRONIK SE & Co. KG
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 III | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- BIOTRONIK SE & Co. KG
Sources (1)
- FDA UDI 73cb08eb-4af5-4c90-85c7-d1f22672a877 35 fields · synced Jun 8, 2026